http://identifiers.org/hco/7/GRCh38#8433654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8948217-C-A

8433654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5 prime UTR variant
orthologous variants: 8948217-C-T

8433693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5 prime UTR variant
orthologous variants: 8948257-C-G

8433763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 8948332-C-T

http://identifiers.org/hco/7/GRCh38#8433827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8948401-C-A

8433827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5 prime UTR variant
orthologous variants: 8948401-C-T

http://identifiers.org/hco/7/GRCh38#8433835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8948409-C-A

8433835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5 prime UTR variant
orthologous variants: 8948409-C-T

8433925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 8948504-G-A

http://identifiers.org/hco/7/GRCh38#8433952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#8948531-C-A

8433968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 8948547-T-C

http://identifiers.org/hco/7/GRCh38#8433998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#8948577-C-A

8433998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 8948577-C-G

8434105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5 prime UTR variant
orthologous variants: 8948685-G-A

http://identifiers.org/hco/7/GRCh38#8434152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8948732-C-A

8434152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5 prime UTR variant
orthologous variants: 8948732-C-T

8434535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5 prime UTR variant
orthologous variants: 8949096-G-A

8434535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5 prime UTR variant
orthologous variants: 8949096-G-T

8434620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5 prime UTR variant
orthologous variants: 8949181-G-A

8434620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5 prime UTR variant
orthologous variants: 8949181-G-T

8434796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8949357-T-C

8434809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, undefined
orthologous variants: 8949370-G-A

8434809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, undefined
orthologous variants: 8949370-G-T

8434865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, undefined
orthologous variants: 8949428-T-C

8434924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8949487-T-C

8435003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8949556-G-T

8435048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8949601-T-C

http://identifiers.org/hco/7/GRCh38#8435123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8949656-C-A

8435123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8949656-C-G

8435123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8949656-C-T

8435134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8949667-G-A

8435134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8949667-G-C

8435134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8949667-G-T

http://identifiers.org/hco/7/GRCh38#8435139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8949672-C-A

8435139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8949672-C-T

8435143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8949676-G-A

8435143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8949676-G-C

8435143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8949676-G-T

http://identifiers.org/hco/7/GRCh38#8435212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8949738-C-A

8435212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8949738-C-T

8435220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8949746-G-A

8435220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8949746-G-T

8435224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8949750-G-A

8435224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8949750-G-C

8435361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8949904-C-G

8435361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8949904-C-T

http://identifiers.org/hco/7/GRCh38#8435530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8950074-C-A

8435530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8950074-C-T

8435774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 8950314-C-T

8435781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8950321-G-T

8435785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8950325-C-T

8435839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8950384-G-A

8435839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8950384-G-T

8435864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8950418-G-A

8435864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8950418-G-C

8435864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8950418-G-T

8435919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8950471-G-T

8436107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8950655-T-A

8436107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8950655-T-C

8436128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8950676-G-T

8436224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8950753-G-A

8436572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8951086-G-A

8436688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8951189-T-G

8436691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8951192-C-G

8436928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8951437-A-G

8437358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, undefined
orthologous variants: 8951867-G-T

8437429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8951944-G-A

http://identifiers.org/hco/7/GRCh38#8438321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8952890-C-A

8438327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8952896-A-G

8438775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8953377-T-A

8438808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8953408-T-G

8438975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8953619-G-A

8439056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8953709-G-A

8439056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8953709-G-C

http://identifiers.org/hco/7/GRCh38#8439132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8953775-A-C

8439138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8953781-G-C

8439138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8953781-G-T

http://identifiers.org/hco/7/GRCh38#8439475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8954112-C-A

8439475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8954112-C-T

8439544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8954182-G-A

8439852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8954405-G-A

8439853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8954406-A-G

8439874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8954411-G-A

8440076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8954607-A-G

8440458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8955000-T-C

8440797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8955337-G-A

8440797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8955337-G-T

8440886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8955430-G-A

8440985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8955551-T-G

8441037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8955609-A-G

8441223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8955946-C-T

http://identifiers.org/hco/7/GRCh38#8441265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8955987-C-A

8441269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8955991-T-C

8441273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8955995-C-G

8441841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8956564-T-A

8441937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8956685-G-T

8442050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8956792-G-A

8442050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8956792-G-T

8442140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8956881-T-C

http://identifiers.org/hco/7/GRCh38#8442212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8956964-C-A

8442379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8957130-T-C

8442593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8957315-A-G

8442642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8957367-C-T

8442722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, undefined
orthologous variants: 8957442-C-T

http://identifiers.org/hco/7/GRCh38#8442788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#8957509-C-A

8442788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, undefined
orthologous variants: 8957509-C-T

8442816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, undefined
orthologous variants: 8957537-G-C

8442816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, undefined
orthologous variants: 8957537-G-T

8442911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, undefined
orthologous variants: 8957637-G-A

8443366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8958045-G-A

8443366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8958045-G-C

8443569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8958267-G-T

http://identifiers.org/hco/7/GRCh38#8443626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8958333-A-C

8443898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8958596-T-C

8443965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8958648-G-C

8444009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8958697-C-G

8444060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8958748-C-T

8444191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8958873-C-T

8444197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8958879-A-G

8444558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8959198-T-C

8444601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8959219-T-C

8444662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8959271-G-T

8444764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8959336-T-C

8444846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8959446-T-A

8445328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8959946-A-G

http://identifiers.org/hco/7/GRCh38#8445683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8960281-A-C

8446138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8960704-G-A

8446337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8960894-G-A

8446431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8960994-A-G

8446442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8961005-T-A

8447289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8961794-G-A

8447289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8961794-G-C

8447305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8961810-T-G

8447366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8961871-A-T

8447688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8962222-T-G

8447757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8962291-T-C

8447814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8962345-T-G

8448005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8962539-G-A

8448110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8962689-C-T

8448138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8962717-G-A

8448185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8962749-G-A

8448267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8962830-C-T

8448943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8963179-G-C

8449091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8963326-G-C

8449115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8963350-G-T

8449262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8963520-T-C

8449271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8963526-T-A

8449292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8963547-G-A

8449298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8963553-C-G

8449298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8963553-C-T

8449312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8963565-G-A

8449776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8964112-C-T

8449781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8964117-C-T

8450002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8964299-C-T

8450043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8964340-G-A

8450186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8964485-G-C

http://identifiers.org/hco/7/GRCh38#8450338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8964638-A-C

8451108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8965432-A-G

8451108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8965432-A-T

8451192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8965517-T-A

8451444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8965764-C-G

8451496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8965803-C-T

8451530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8965837-C-T

8451842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8966069-A-G

8451929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8966146-A-G

8452000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8966218-A-T

http://identifiers.org/hco/7/GRCh38#8452290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8966643-C-A

8452290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8966643-C-T

8452335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8966705-C-T

8452395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8966766-C-G

8452395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8966766-C-T

8452467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8966850-G-A

8452923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8967297-T-C

8453308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8967676-A-G

8453479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8967854-T-C

8454343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8968330-T-C

8454356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8968343-A-G

8454381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8968368-G-A

8454398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8968378-C-T

8454622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8969002-C-T

8454683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8969067-C-T

8454739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8969125-C-G

8454756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8969144-A-G

http://identifiers.org/hco/7/GRCh38#8454774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8969162-A-C

8454881-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8969255-T-A

8455062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8969396-A-G

8455062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8969396-A-T

8455110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8969443-A-G

8455217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8969545-G-A

8455302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8969621-T-C

8455302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8969621-T-G

8455379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8969699-G-C

8455802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8970122-A-T

8455885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8970202-A-T

8455979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8970287-G-A

8456053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8970355-C-T

8456341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8970615-T-C

8456805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8971702-C-T

8456841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8971735-C-T

8457155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8972031-G-A

8457213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8972087-C-G

8457213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8972087-C-T

http://identifiers.org/hco/7/GRCh38#8457300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8972219-C-A

8457319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8972238-T-A

http://identifiers.org/hco/7/GRCh38#8457473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8972414-C-A

http://identifiers.org/hco/7/GRCh38#8457579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8972523-A-C

8457753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8972696-T-C

8457925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8972880-T-C

8458489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8973608-C-T

8458804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8973913-T-C

8458845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8973956-T-C

8458855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8973965-C-G

8458889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8973996-A-G

8458964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8974084-A-G

http://identifiers.org/hco/7/GRCh38#8459039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8974144-C-A

8459303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8974403-T-A

http://identifiers.org/hco/7/GRCh38#8459322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8974422-C-A

8459369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8974469-T-C

8459462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8974562-T-C

8459507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8974607-C-T

8459629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8974725-T-A

8459692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8974788-C-T

8459759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8974842-G-C

8459771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8974854-C-T

8459943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8975020-G-A

8459957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8975034-C-G

8460042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8975083-C-G

8460256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8975285-C-T

8460268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8975298-C-T

8460291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8975320-C-T

8460363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8975379-C-G

8460363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8975379-C-T

8460458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8975469-C-T

8460519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8975530-G-T

8460528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8975920-G-C

8460611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8976580-G-A

8460703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8976643-T-G

8460792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8976739-C-G

8460902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8976843-C-G

http://identifiers.org/hco/7/GRCh38#8460969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8976894-C-A

8460969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8976894-C-T

8461176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8977072-C-T

http://identifiers.org/hco/7/GRCh38#8461255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8977142-C-A

8461263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8977150-C-T

8461307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8977190-C-T

8464810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8978694-C-G

8464810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8978694-C-T

8464847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8978731-G-T

8464907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8978787-G-A

8465144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8979034-C-T

8465234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8979119-G-T

http://identifiers.org/hco/7/GRCh38#8465289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8979175-C-A

8465289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8979175-C-T

8465323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8979208-A-G

8465324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8979209-T-G

8465354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8979239-T-G

8465410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8979293-C-T

8465414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8979297-C-G

8465444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8979327-C-T

8465471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8979353-G-A

8465471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8979353-G-C

8465498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8979380-C-T

8465681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8979563-A-G

http://identifiers.org/hco/7/GRCh38#8465777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8979659-A-C

8465777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8979659-A-G

8465777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8979659-A-T

8465823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8979705-G-A

8465958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8979795-G-A

8465972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8979809-G-C

8466070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8979919-A-G

8466517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8980370-A-T

8466669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8980525-G-A

8466763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8980595-T-A

8466796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8980631-T-C

8466854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8980668-G-A

8466870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8980677-C-G

8466970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8980773-G-T

8467017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8980812-G-A

8467143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8980971-T-A

8467346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8981175-T-A

8467410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8981239-G-A

8467410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8981239-G-C

8467524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8981352-T-C

8467806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8981660-A-T

8467924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8981779-T-A

http://identifiers.org/hco/7/GRCh38#8468142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8982008-A-C

8468274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8982141-T-G

8468291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8982158-C-T

8468297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8982167-A-G

8469976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8982234-T-G

8470031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8982288-G-A

8470134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8982382-T-G

8470383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8982625-C-G

8470383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8982625-C-T

8470456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8982690-G-C

8470601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8982838-G-T

8470624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8982861-G-A

8470624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8982861-G-C

8470624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8982861-G-T

8470627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8982864-G-C

8471381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8983566-A-G

8471491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8983681-G-C

8471561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8983787-T-C

8471873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8984274-A-G

8471989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8984414-G-C

8472149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8984556-T-C

http://identifiers.org/hco/7/GRCh38#8472435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8984840-A-C

8472435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8984840-A-G

8472493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8984891-C-G

8472503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8984901-G-T

8472555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8984972-G-A

8472598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8985014-G-A

8472663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8985090-A-G

8472878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8985489-C-G

8472878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8985489-C-T

8472970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8985584-T-G

8473005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8985618-C-T

8473039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8985641-T-C

8473110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8985703-G-A

8473110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8985703-G-C

http://identifiers.org/hco/7/GRCh38#8473185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8985777-A-C

8473185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8985777-A-T

8473229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8985821-T-C

8473256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8985848-G-A

8473256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8985848-G-C

8473283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8985868-T-C

http://identifiers.org/hco/7/GRCh38#8473519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8986094-C-A

8473624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8986201-C-T

http://identifiers.org/hco/7/GRCh38#8473658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8986232-A-C

8473658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8986232-A-G

http://identifiers.org/hco/7/GRCh38#8473848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8986393-C-A

8473848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8986393-C-T

8473984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8986454-G-C

8474027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8986497-C-G

8474027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8986497-C-T

8474046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8986516-A-T

8474076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8986547-C-G

8474185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8986650-G-C

8474209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8986679-T-A

http://identifiers.org/hco/7/GRCh38#8474279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8986744-A-C

8474477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8986976-C-G

8474478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8986977-T-C

8474494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8986989-C-T

8474677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8987189-A-G

http://identifiers.org/hco/7/GRCh38#8474779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8987782-A-C

8474779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8987782-A-G

8474880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8987885-G-A

8475050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8988050-G-T

8475265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8988859-G-A

8475265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8988859-G-C

http://identifiers.org/hco/7/GRCh38#8475465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8989049-C-A

8475469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8989053-T-A

8475551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8989134-G-T

8475553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8989136-A-G

http://identifiers.org/hco/7/GRCh38#8475562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8989145-A-C

8475564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8989147-G-A

8475564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8989147-G-T

8475617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8989195-T-A

8475760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8989298-T-C

8475827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8989387-G-A

8475827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8989387-G-T

http://identifiers.org/hco/7/GRCh38#8475959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8989542-C-A

8476029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8989616-T-G

8476187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8989750-A-T

http://identifiers.org/hco/7/GRCh38#8476190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8989753-C-A

8477344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8990013-T-A

8477345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8990014-A-T

8477399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8990056-G-A

8477404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8990061-C-G

8477560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8990215-A-G

8477697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8990766-G-A

8477766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8990834-G-T

8477849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8990910-C-T

8477948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8990994-T-C

8478050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8991095-T-C

8478102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8991142-C-T

8478159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8991205-G-A

8478159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8991205-G-T

8478316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8991307-A-G

8478317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8991308-T-C

8478374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8991365-G-C

8478447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8991479-T-C

http://identifiers.org/hco/7/GRCh38#8478613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8991857-C-A

8478613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8991857-C-T

8478627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8991878-T-G

8478730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8991994-C-T

8478945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8992208-C-T

8478986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8992247-A-G

8479018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8992278-A-G

8479339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8992538-A-G

http://identifiers.org/hco/7/GRCh38#8479720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8992895-C-A

8480116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8994409-A-G

8480177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8994463-G-A

8480179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8994465-A-G

8480251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8994538-T-A

8480251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8994538-T-G

8480882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8995157-T-C

8481235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8995886-A-T

8481243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8995894-T-C

8481259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8995910-T-A

8481915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8996423-G-T

8481940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8996448-A-G

8482003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8996506-C-G

8482183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8996690-G-A

8482202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8996710-G-A

8482208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8996716-G-A

8482208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8996716-G-C

8482208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8996716-G-T

8482379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8996887-T-A

8482462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8996970-T-C

8482518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8997023-C-T

8482549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8997054-C-G

8482549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8997054-C-T

8482652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8997143-A-G

8482658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8997149-C-G

8483111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8997593-A-G

8483189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8997652-G-C

8483645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8998002-G-T

8483689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8998063-G-C

8483741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8998104-C-T

8483749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8998112-G-C

http://identifiers.org/hco/7/GRCh38#8483879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8998269-C-A

8483943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8998333-G-A

8483943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8998333-G-T

8483984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8998366-A-T

8483985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8998367-G-A

8483985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8998367-G-T

8484158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8998530-C-T

8484258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8998629-T-C

8484559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8999263-G-A

8484559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8999263-G-T

8484705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8999406-G-T

8484746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 8999444-T-C

8485532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9000250-G-T

8485628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9000333-T-C

8485654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9000357-G-A

8485659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9000362-G-C

8485820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9000539-G-C

8485849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9000568-A-G

8485917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9000656-G-T

8487945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9001547-T-C

8488084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9001683-T-A

8488156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9001747-T-G

8488198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9001779-T-G

8488209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9001781-C-T

8488280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9001814-C-T

http://identifiers.org/hco/7/GRCh38#8488308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9001840-A-C

8488469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9002008-C-G

8488499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9002038-G-A

8488499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9002038-G-T

8488550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9002085-G-T

8489080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9002605-T-G

8489125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9002648-G-A

8489189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9002707-G-T

8489202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9002719-A-G

8489212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9002734-G-A

8489281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9002770-G-A

http://identifiers.org/hco/7/GRCh38#8489367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9002854-C-A

8489540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9002935-C-T

8489570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9002966-C-T

http://identifiers.org/hco/7/GRCh38#8489676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9003050-C-A

8489760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9003136-T-C

8489760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9003136-T-G

http://identifiers.org/hco/7/GRCh38#8489763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9003139-C-A

8489799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9003213-A-G

8489828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9003242-A-G

8489832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9003246-A-G

http://identifiers.org/hco/7/GRCh38#8489836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9003252-A-C

http://identifiers.org/hco/7/GRCh38#8489902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9003336-C-A

8489902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9003336-C-T

8490082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9003498-T-C

8490142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9003559-A-G

8490190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9003593-A-G

8490332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9003722-C-T

8490482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9003828-G-A

8490491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9003837-A-G

8490499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9003845-G-A

8490537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9003848-G-A

8490544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9003856-G-A

8490590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9003890-G-A

8490591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9003891-C-T

8490592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9003892-G-A

8490796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9004103-G-A

8490819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9004126-C-G

8490819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9004126-C-T

http://identifiers.org/hco/7/GRCh38#8490936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9004260-C-A

8490970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9004292-G-A

8491044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9004362-C-G

8491073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9004394-T-C

8491074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9004395-G-T

8491147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9004467-G-T

8491695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9005005-C-T

8491788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9005088-A-G

8491792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9005092-A-T

8491814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9005114-C-T

8492236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9005544-C-T

8492267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9005575-G-C

8492323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9005626-C-G

8492403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9005711-A-G

http://identifiers.org/hco/7/GRCh38#8492589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9005898-A-C

8492616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9005925-T-C

8492780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9006077-A-G

8492908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9006205-C-T

8493108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9006404-G-A

8493182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9006479-T-C

8493330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9006633-G-A

8493334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9006637-G-A

8493337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9006641-G-T

8493359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9006661-G-T

8493476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9006775-C-G

8493476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9006775-C-T

8493559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9006868-G-A

8493915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9007249-G-A

8493941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9007292-C-G

8493957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9007303-T-C

8494025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9007366-G-A

8494030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9007371-G-T

8494039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9007380-T-C

8494131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9007462-T-A

8494880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9008565-G-A

8494953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9008624-C-G

8496015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9009421-G-A

8496020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9009426-C-G

http://identifiers.org/hco/7/GRCh38#8496408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9009781-C-A

8498146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9012755-C-T

http://identifiers.org/hco/7/GRCh38#8498201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9012805-A-C

8498559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9013178-C-T

8498764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9013386-T-C

8498868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9013503-G-C

8499012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9013551-G-A

8499336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9015013-G-C

8499336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9015013-G-T

8499358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9015036-C-T

8499454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9015128-G-A

8499573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9015262-A-G

8499705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9015343-C-G

8499705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9015343-C-T

8500492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9016809-G-A

8500492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9016809-G-T

8500561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9016876-G-C

8500611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9016926-G-A

8500868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9017163-T-C

8500986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9017261-C-T

8501003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9017278-A-T

8501154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9017436-A-G

8501284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9017566-G-T

http://identifiers.org/hco/7/GRCh38#8501354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9017640-A-C

8501358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9017644-C-G

http://identifiers.org/hco/7/GRCh38#8501470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9017749-A-C

8501470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9017749-A-G

8501663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9017949-C-G

8501673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9017958-G-A

8501708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9017990-A-G

8502074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9018203-C-G

8502173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9018310-A-G

8502225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9018362-G-T

8504955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9018938-G-A

8505002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9018978-G-T

8505033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9019008-A-T

8505149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9019124-G-A

http://identifiers.org/hco/7/GRCh38#8505234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9019210-A-C

http://identifiers.org/hco/7/GRCh38#8505316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9019293-C-A

http://identifiers.org/hco/7/GRCh38#8505383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9019360-A-C

8505383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9019360-A-G

8505437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9019413-A-G

http://identifiers.org/hco/7/GRCh38#8505489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9019428-C-A

8505600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9019522-G-A

8505829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9019722-G-A

8505829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9019722-G-T

8506039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9021074-T-C

8506056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9021090-A-T

8506177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9021206-T-A

8506253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9021281-T-C

8506352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9021445-C-G

8506366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9021451-G-A

8506531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9021598-A-G

8506571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9021638-G-C

8506806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9021773-C-T

8506961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9021923-T-C

8507010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9021948-T-A

8507010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9021948-T-C

8507274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9022113-A-G

8507363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9022209-C-G

8507365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9022211-G-T

8507580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9022432-G-A

8507682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9022532-A-G

8507973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9022832-G-A

8508320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9023174-T-G

8508326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9023180-T-A

8508693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9023497-A-G

8508693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9023497-A-T

8508835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9023624-G-A

8509063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9023894-G-T

8509080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9023911-T-C

8509320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9024134-T-A

8509423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9024237-G-C

8509456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9024400-T-C

http://identifiers.org/hco/7/GRCh38#8509490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9024464-C-A

8509490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9024464-C-T

8509501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9024469-A-G

8509520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9024487-T-C

8509531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9024498-G-A

8509547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9024512-T-C

8509650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9024616-C-T

8509652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9024618-G-C

8509714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9024679-T-A

8509766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9024730-C-G

8509841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9024802-G-A

8509955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9024913-G-A

8510437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9025350-T-C

8510687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9025499-G-A

8511174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9026535-A-G

8511230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9026591-G-T

8511241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9026602-C-T

8511309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9026672-A-G

8511381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9026741-C-T

8511618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9026981-G-A

8511794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9027124-C-T

8511827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9027142-G-T

8512075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9027390-C-T

8512739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9027867-T-C

8514022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9028694-C-G

8514147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9028808-C-T

http://identifiers.org/hco/7/GRCh38#8514530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9029103-C-A

8514564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9029135-A-G

8514626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9029197-C-G

8515103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9029642-G-T

8515183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9029723-C-T

8515399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9029939-T-C

8515437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9029978-G-A

8515533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9030120-G-A

8515533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9030120-G-T

8515909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9030648-C-G

8516005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9033242-C-G

8516005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9033242-C-T

8516118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9033350-G-A

8516149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9033373-T-C

8516342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9033565-G-A

8516400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9033621-T-A

8516540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9033743-A-G

8516540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9033743-A-T

8516572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9033775-A-G

8516644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9033845-T-C

8516701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9033903-A-G

8516969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9034150-G-C

8517172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9034349-T-A

8517312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9034482-G-C

8517416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9034568-T-A

8517712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9034845-G-A

8517712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9034845-G-C

8518026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9035134-G-T

8518029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9035137-C-T

8518144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9035244-A-T

8518383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9035445-A-G

8518461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9035481-G-T

8518466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9035486-C-T

8518922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9035743-A-G

8518922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9035743-A-T

8518933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9035764-C-T

8518952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9035781-A-G

8519024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9035848-G-A

8519109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9035902-G-A

8519123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9035915-C-T

8519248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9036038-T-G

8519330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9036125-C-G

8519330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9036125-C-T

8519384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9036176-A-G

8519428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9036217-G-A

8519559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9036461-A-G

8519627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9036520-A-G

8519651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9036544-T-C

http://identifiers.org/hco/7/GRCh38#8519666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9036559-C-A

8519666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9036559-C-G

8519695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9036571-G-A

8519695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9036571-G-T

8519982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9036837-T-A

8520067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9036917-A-G

8520235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9037075-G-A

8520273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9037112-T-A

8520274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9037113-G-C

8520274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9037113-G-T

8520286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9037125-C-G

8521090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9037909-T-C

8521368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9038586-A-G

8521368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9038586-A-T

8521623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9038796-T-C

8521636-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9038805-A-T

8521671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9038846-G-C

8521982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9039121-G-C

8522010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9039228-G-A

8522232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9039427-C-T

8522261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9039465-T-C

8522415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9039607-A-G

8522415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9039607-A-T

8522425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9039617-A-G

8522630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9039822-T-C

8522784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9039977-G-T

8522879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9040057-A-G

8523163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9040311-T-A

8523182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9040330-G-A

8523292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9040442-T-C

http://identifiers.org/hco/7/GRCh38#8523378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9040531-C-A

8523378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9040531-C-T

8523397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9040546-T-C

8523448-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9040597-T-A

8523460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9040610-G-T

8523483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9040628-A-G

http://identifiers.org/hco/7/GRCh38#8523533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9040680-C-A

8523566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9040715-T-C

8523584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9040733-G-A

8523664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9040800-A-G

8523701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9040842-A-T

8523910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9041016-G-A

8527202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9041609-T-C

8527257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9041653-C-T

8527258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9041654-G-A

8527277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9041670-C-T

8527321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9041716-A-T

8527332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9041725-C-T

8527412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9041788-A-G

http://identifiers.org/hco/7/GRCh38#8527414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9041790-A-C

8527500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9041877-C-T

8527545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9041916-G-A

8527656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9042012-G-T

8527689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9042052-T-C

http://identifiers.org/hco/7/GRCh38#8527794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9042153-A-C

8528049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9042372-T-A

8528163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9042467-G-C

8528309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9042611-G-T

8528405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9042693-C-T

http://identifiers.org/hco/7/GRCh38#8528529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9042819-C-A

8528600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9042877-G-T

8528669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9042954-C-T

8529002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9043279-T-G

8529114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9045190-T-C

8529118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9045194-T-G

8529131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9045207-G-T

8529158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9045229-T-C

8529198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9045270-G-A

8529269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9045346-A-G

8529324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9045403-G-A

8529324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9045403-G-C

8529380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9045461-C-T

http://identifiers.org/hco/7/GRCh38#8529481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9045565-A-C

8529532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9045612-A-G

8529586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9045655-T-G

http://identifiers.org/hco/7/GRCh38#8529796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9045804-C-A

8529796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9045804-C-T

8529813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9045821-G-A

8529813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9045821-G-T

8529814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9045822-G-T

8529882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9045890-A-G

8530098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9046173-C-T

8530191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9046285-G-A

http://identifiers.org/hco/7/GRCh38#8530252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9046411-C-A

8530253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9046412-T-C

8530326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9046537-C-T

8530332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9046543-G-A

8530438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9046658-T-A

8530438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9046658-T-C

8530658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9046999-G-A

8531186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9047517-T-C

8531357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9047636-T-C

8531721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9047959-A-G

http://identifiers.org/hco/7/GRCh38#8532124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9048344-C-A

8532124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9048344-C-T

8532142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9048362-C-G

8532380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9048601-C-G

8532380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9048601-C-T

8532498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9048708-G-T

8532550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9048747-C-T

8532663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9048846-C-G

http://identifiers.org/hco/7/GRCh38#8532781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9048972-C-A

8532809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9048983-G-A

8532809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9048983-G-T

http://identifiers.org/hco/7/GRCh38#8533003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9049160-C-A

8533126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9049282-G-A

http://identifiers.org/hco/7/GRCh38#8533310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9049904-A-C

8533312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9049906-A-G

8533402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9049964-T-C

8533402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9049964-T-G

8533422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9049984-T-C

http://identifiers.org/hco/7/GRCh38#8533513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9050072-C-A

8533675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9050216-T-C

8533748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9050287-C-T

8533980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9050526-A-T

8534155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9050698-C-G

8534807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9051329-T-C

8534899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9051410-C-T

8534960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9051470-G-A

http://identifiers.org/hco/7/GRCh38#8535008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9051525-A-C

8535008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9051525-A-G

8535115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9051689-G-A

8535295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9051844-G-A

8535516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9052029-G-A

8535516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9052029-G-T

http://identifiers.org/hco/7/GRCh38#8535574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9052099-C-A

8535728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9053470-A-T

8535733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9053475-T-A

8535804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9053539-G-T

8535812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9053547-T-G

http://identifiers.org/hco/7/GRCh38#8535827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9053566-A-C

8535892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9053621-T-A

8535939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9053665-G-A

8535939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9053665-G-T

8536012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9053737-C-G

8536108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9053831-C-T

8536384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9054112-C-T

8536400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9054125-A-T

8536492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9054216-G-C

8536586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9054315-G-T

http://identifiers.org/hco/7/GRCh38#8536649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9054379-A-C

http://identifiers.org/hco/7/GRCh38#8536729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9054461-A-C

8536733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9054465-T-A

8536749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9054481-A-G

8536788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9054515-T-C

8536799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9054525-T-C

8536815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9054541-G-A

8537045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9054750-A-G

http://identifiers.org/hco/7/GRCh38#8538383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9055927-A-C

8538506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9056051-G-C

8538514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9056059-A-G

8538752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9056283-T-C

http://identifiers.org/hco/7/GRCh38#8538839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9056369-C-A

http://identifiers.org/hco/7/GRCh38#8539060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9056557-A-C

8539062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9056559-C-T

8539443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9056885-T-A

8539443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9056885-T-C

8539471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9056932-T-C

8539751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9057202-T-A

http://identifiers.org/hco/7/GRCh38#8539811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9057263-A-C

8539811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9057263-A-G

8539885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9057332-T-C

8540059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9057495-C-G

8540188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9057627-G-T

8540264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9057751-C-G

8540560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9058120-G-A

8542811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9058798-A-G

8543305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9061183-C-G

8543305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9061183-C-T

8543323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9061199-T-C

8543392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9061263-A-T

8543402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9061273-C-G

8543464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9061331-T-C

8543486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9061345-G-T

8543607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9061464-C-T

8543737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9061582-T-C

8543837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9061730-A-G

8544022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9061907-G-C

http://identifiers.org/hco/7/GRCh38#8544034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9061921-C-A

8544034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9061921-C-T

8544056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9061943-C-T

8544152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9062024-G-A

8544344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9062201-T-G

8544523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9062357-C-T

8544610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9062444-G-A

8544667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9062501-T-C

8544668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9062502-G-A

8544668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9062502-G-C

8544688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9062522-A-G

8544688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9062522-A-T

8544721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9062558-G-A

8544721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9062558-G-C

8544729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9062566-T-C

8544729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9062566-T-G

8544853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9062684-T-C

8544853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9062684-T-G

8544977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9062796-G-C

8545006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9062830-C-G

8545006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9062830-C-T

8545149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9062951-G-A

8545213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9063025-A-T

8545573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9063346-A-G

8545592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9063364-T-C

8545745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9063519-C-T

8545772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9063546-A-G

8545789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9063563-C-G

8545841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9063620-A-G

8546001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9063774-C-T

http://identifiers.org/hco/7/GRCh38#8546067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9063840-C-A

8546181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9063957-G-A

8546250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9064032-G-A

8546334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9064131-C-T

8546393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9064190-G-A

8546550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9064510-G-A

8546587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9064542-T-C

8546966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9065125-G-A

8547115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9065258-C-T

http://identifiers.org/hco/7/GRCh38#8547147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9065289-C-A

8547147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9065289-C-G

8547147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9065289-C-T

8548175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9065596-C-G

8548381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9065766-C-T

8548927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9066277-G-T

8549143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9066479-C-T

http://identifiers.org/hco/7/GRCh38#8549382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9066722-A-C

8549382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9066722-A-G

8549662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9067018-G-A

8549662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9067018-G-C

8549812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9067156-T-C

http://identifiers.org/hco/7/GRCh38#8549920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9067264-C-A

8550056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9067399-C-G

8550090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9067433-A-G

8550221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9067563-C-T

8550490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9067847-G-T

8551872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9068261-T-C

8552601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9068948-T-C

8552620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9068967-A-G

http://identifiers.org/hco/7/GRCh38#8553876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9069684-A-C

8554061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9069851-A-G

8554061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9069851-A-T

8554226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9070006-C-T

http://identifiers.org/hco/7/GRCh38#8554962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9070328-A-C

8555014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9070380-T-C

8555161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9070537-G-T

8555324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9070699-G-T

8555381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9070756-C-G

8555381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9070756-C-T

8555422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9070797-C-T

8556110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9071496-C-G

8556132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9071519-G-A

8556734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9071928-G-A

8556811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9072005-G-A

8556811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9072005-G-C

8556948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9072103-G-A

8557127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9072250-T-C

8557144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9072265-T-C

http://identifiers.org/hco/7/GRCh38#8557222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9072335-A-C

8557222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9072335-A-G

8557501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9072567-T-C

8557569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9072636-G-A

8557677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9072746-A-G

8557685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9072754-C-T

8557836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9072897-C-G

8557854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9072915-T-A

8557913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9072957-A-T

8557915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9072959-C-G

8557915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9072959-C-T

8558086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9073073-C-G

8558214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9073180-C-G

http://identifiers.org/hco/7/GRCh38#8558443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9073473-C-A

8558616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9074181-C-G

8559397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9074534-C-T

8559462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9074615-C-T

8559838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9074986-G-A

8559848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9074996-T-C

8559855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9075003-C-T

8559990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9075158-C-T

http://identifiers.org/hco/7/GRCh38#8560010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9075175-C-A

8560011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9075176-G-C

http://identifiers.org/hco/7/GRCh38#8560013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9075183-C-A

8560070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9075237-G-A

8560070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9075237-G-C

8560095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9075262-C-T

8560113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9075273-C-G

http://identifiers.org/hco/7/GRCh38#8560116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9075276-A-C

8560248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9075400-C-T

8560606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9075762-A-T

8560665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9075822-C-G

8560690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9075847-C-G

8560892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9076040-G-T

8560985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9076135-G-A

8561119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9076269-T-C

8561190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9076342-G-A

http://identifiers.org/hco/7/GRCh38#8561282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9076436-A-C

8561336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9076522-G-A

8561336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9076522-G-C

8561338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9076524-G-A

8561402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9076555-C-T

8561428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9076571-C-T

8561619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9076761-C-G

http://identifiers.org/hco/7/GRCh38#8561656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9076795-C-A

8561854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9076960-A-G

8561937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9077024-G-A

8563629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9077709-T-C

8563666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9077747-T-C

8563793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9077840-C-T

8563969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9078018-C-T

8563999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9078048-A-G

http://identifiers.org/hco/7/GRCh38#8564237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9078277-C-A

8564237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9078277-C-G

8564556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9078599-G-A

8564556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9078599-G-T

8564602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9078645-A-G

8564799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9078849-T-C

8564907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9078945-A-G

http://identifiers.org/hco/7/GRCh38#8564979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9079010-C-A

8564984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9079015-A-G

8565093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9079078-C-T

8565158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9079141-C-G

8565286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9079268-A-G

8565299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9079280-A-G

8565312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9079293-G-A

8565312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9079293-G-T

8565340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9079321-G-A

8565340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9079321-G-T

8565432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9079422-T-A

8566189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9079899-G-A

8566189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9079899-G-C

8566223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9079931-A-G

8568089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9081413-A-G

8568099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9081423-T-C

8568160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9081484-C-G

8568508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9081835-C-G

8568508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9081835-C-T

8568608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9081930-T-A

http://identifiers.org/hco/7/GRCh38#8568735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9082040-C-A

8568735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9082040-C-T

8568900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9082189-A-G

http://identifiers.org/hco/7/GRCh38#8568948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9082245-A-C

8570385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9082713-T-A

8570492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9082841-T-C

http://identifiers.org/hco/7/GRCh38#8570680-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9083064-A-C

8570798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9083176-A-G

8570847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9083226-T-C

8570866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9083249-A-G

8570866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9083249-A-T

http://identifiers.org/hco/7/GRCh38#8571156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9083456-C-A

8571205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9083504-A-G

8571211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9083510-T-C

8571321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9083594-G-A

8571335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9083608-T-C

8571345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9083616-G-A

8571358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9083629-A-G

8571371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9083634-C-T

8571375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9083638-T-C

8571393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9083656-T-C

8572076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9084312-T-G

8572122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9084365-T-G

8572131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9084374-C-T

8572204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9084446-C-G

http://identifiers.org/hco/7/GRCh38#8572259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9084497-C-A

8572265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9084503-T-G

8572822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9085062-A-G

http://identifiers.org/hco/7/GRCh38#8573021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9085247-C-A

8573021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9085247-C-T

8573131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9085322-A-G

8573191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9085338-A-T

8573224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9085377-A-G

8573450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9085617-G-A

8573697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9085881-C-T

8573823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9086008-C-G

8574002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9086186-C-G

8574231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9086431-A-G

8574255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9086455-A-G

8574771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9087247-G-A

http://identifiers.org/hco/7/GRCh38#8574825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9087289-C-A

http://identifiers.org/hco/7/GRCh38#8575148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9087609-C-A

8575148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9087609-C-T

8575279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9087742-C-G

8575285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9087748-T-G

8575335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9087797-C-G

8575424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9087886-T-C

http://identifiers.org/hco/7/GRCh38#8575485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9087947-A-C

8575509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9087970-T-C

8575526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9087988-C-T

8575544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9087999-C-T

8575798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9088956-C-T

8575895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9089057-C-T

8576262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9089406-T-C

http://identifiers.org/hco/7/GRCh38#8576308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9089452-C-A

8576308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9089452-C-T

http://identifiers.org/hco/7/GRCh38#8576351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9089493-C-A

8576446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9089588-T-G

8576469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9089611-T-C

8576592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9089711-G-A

8576592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9089711-G-C

http://identifiers.org/hco/7/GRCh38#8576679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9089802-A-C

8576688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9089811-C-T

8576689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9089812-T-C

8576932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9090039-G-C

8576997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9090108-A-G

8577286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9090373-G-T

8577310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9090396-C-G

http://identifiers.org/hco/7/GRCh38#8577323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9090409-C-A

8577522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9090599-C-T

8577538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9090617-G-A

8577679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9090733-C-T

8577758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9090796-G-A

8577981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9091046-C-T

8578010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9091073-A-G

8578763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9091657-G-A

8579182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9092057-T-C

8579196-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9092071-T-A

8579233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9092104-G-A

http://identifiers.org/hco/7/GRCh38#8580443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9094026-C-A

8580496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9094079-G-C

8580750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9094335-T-G

8580863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9094455-A-T

8580966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9094565-G-A

8581005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9094603-C-T

8581138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9094717-G-A

8581138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9094717-G-C

8584462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9095819-T-G

8584567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9095926-A-G

8584577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9095936-G-A

8584577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9095936-G-C

8584667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9096021-T-A

8584712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9096064-G-A

8584731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9096082-A-T

8585137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9096490-C-G

8585137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9096490-C-T

8585144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9096497-T-G

8585176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9096538-A-G

http://identifiers.org/hco/7/GRCh38#8585703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9097508-A-C

8585703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9097508-A-G

http://identifiers.org/hco/7/GRCh38#8585784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9097589-C-A

8585784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9097589-C-G

8585911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9097716-G-A

http://identifiers.org/hco/7/GRCh38#8586181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9097951-A-C

8586181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9097951-A-G

8586274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9098042-G-A

8586358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9098116-T-A

8586405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9098163-T-C

8586509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9098266-G-T

8586829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9098574-T-G

8587205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9098950-C-T

8588521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099202-C-G

8588521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099202-C-T

8588558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099239-C-T

8588722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099368-G-C

8588728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099374-C-T

8588766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099385-C-G

8588766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099385-C-T

8589113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099774-T-C

8589162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099823-G-A

8589164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099825-G-A

http://identifiers.org/hco/7/GRCh38#8589327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9099987-A-C

8589390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9100050-T-C

http://identifiers.org/hco/7/GRCh38#8589469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9100129-C-A

8589525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9100172-G-A

8589525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9100172-G-C

8589525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9100172-G-T

8589917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9101262-A-G

http://identifiers.org/hco/7/GRCh38#8590004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9101360-A-C

8590333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9101744-G-A

8590410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9101827-C-G

8590485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9101895-A-G

8590641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9102019-T-C

8591350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9102823-A-G

8591449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9102975-T-C

http://identifiers.org/hco/7/GRCh38#8591461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9102987-A-C

8591461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9102987-A-G

8591467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9102993-G-A

8591638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9103165-G-C

8591649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9103172-C-T

8591685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9103213-A-T

8591691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9103219-A-G

8591796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9103318-C-G

8592105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9103564-T-C

8592239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9103672-G-A

8592411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9103789-A-G

8592501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9103852-T-A

8592501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9103852-T-C

http://identifiers.org/hco/7/GRCh38#8592630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9103961-C-A

http://identifiers.org/hco/7/GRCh38#8593251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9104239-C-A

8593251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9104239-C-T

8593391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9104376-C-G

8593391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9104376-C-T

8593774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9104772-T-C

8594161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9105161-G-A

8594216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9105221-C-T

8594294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9105299-T-C

8594446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9105426-A-T

8594586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9105564-G-C

8594640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9105635-G-A

8594640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9105635-G-C

8594640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9105635-G-T

8594668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9105663-C-G

8594877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9105892-A-G

8594986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9106003-G-C

8595253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9106398-C-T

8595447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9109738-G-A

http://identifiers.org/hco/7/GRCh38#8595877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9110149-C-A

8595935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9110202-G-T

http://identifiers.org/hco/7/GRCh38#8595990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9110261-C-A

8596066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9110332-A-G

8596145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9110411-T-C

8596326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9110580-A-G

http://identifiers.org/hco/7/GRCh38#8596482-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9110735-A-C

8596599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9110853-A-G

8596684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9110927-T-C

8596702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9110944-T-G

8596742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9110977-G-A

8596742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9110977-G-T

8596945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9113399-G-C

8596945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9113399-G-T

8597038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9113458-G-A

8597090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9113510-G-A

8597274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9113673-G-A

8597274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9113673-G-C

8597326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9113726-G-A

8597326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9113726-G-C

8597326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9113726-G-T

8597415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9113787-T-A

8597468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9113850-A-T

8597615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9114068-T-A

8597692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9114144-A-G

8597719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9114162-G-A

8597719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9114162-G-C

8597755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9114190-T-C

8597759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9114194-C-T

8597841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9114276-C-T

8598296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9114730-C-G

8598603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9115025-G-A

8598603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9115025-G-C

8598626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9115050-T-A

8598645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9115065-A-G

8598693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9115112-T-G

8598835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9115239-A-G

8598846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9115252-G-A

8598847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9115253-C-G

8598915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9115320-T-A

8599124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9115534-G-C

8599291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9115698-G-A

8599724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9116121-G-C

http://identifiers.org/hco/7/GRCh38#8599727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9116123-C-A

8599881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9116273-C-T

8599923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9116312-G-A

8599997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9116386-C-G

8600048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9116429-A-G

8600568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9116957-C-T

8600669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9117061-C-T

8600696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9117088-T-A

8600826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9117195-G-T

8601341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9117629-G-C

8601592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9119121-A-G

8601753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9119243-A-T

8601792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9119275-C-G

8601951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9119436-C-G

8601951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9119436-C-T

8602219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9119691-C-T

8603153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9120309-A-G

8603441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9120603-C-T

8603995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9121279-T-C

8604098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9121381-C-G

8604098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9121381-C-T

8604124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9121406-G-C

8604215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9121509-G-T

8604365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9122471-C-G

8604856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9122962-C-T

http://identifiers.org/hco/7/GRCh38#8604952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9123048-C-A

8604952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9123048-C-T

8605009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9123100-T-A

8605138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9123218-G-T

8605154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9123234-C-G

8605154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9123234-C-T

8605174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9123254-A-G

8605424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9123505-C-T

http://identifiers.org/hco/7/GRCh38#8605525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9123604-A-C

8605690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9123767-G-A

8605863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9123937-A-G

8606339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9124500-A-G

8606499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9124660-G-C

8606562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9124723-A-T

8606571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9124732-T-C

8606959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9125121-A-G

8607142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9125442-C-T

8607932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9126117-G-A

8608874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9126566-C-G

8609212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9126711-G-A

8609719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9127027-T-C

8609856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9127153-C-T

8609867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9127164-G-A

8611485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9127978-G-A

http://identifiers.org/hco/7/GRCh38#8611531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9128025-A-C

8611779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9128144-T-G

8612496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9128795-A-G

8612762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9129097-C-G

8612825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9129166-T-C

8612902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9129251-C-G

8612929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9129275-C-T

http://identifiers.org/hco/7/GRCh38#8613094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9129415-C-A

8613094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9129415-C-T

8613230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9129537-G-A

8613618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9129940-C-T

8613690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9130010-A-G

http://identifiers.org/hco/7/GRCh38#8613756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9130077-A-C

8613756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9130077-A-G

8613828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9130132-C-T

http://identifiers.org/hco/7/GRCh38#8613832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9130136-C-A

8613832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9130136-C-G

8614122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9130483-A-G

8614157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9130527-T-C

8614395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9130739-G-T

8614743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9130935-G-T

8614831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9131022-T-C

8615213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9131420-G-A

http://identifiers.org/hco/7/GRCh38#8615261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9131467-C-A

8615276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9131482-A-G

8615433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9131611-G-A

8615468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9131631-C-G

8615473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9131636-A-G

http://identifiers.org/hco/7/GRCh38#8615475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9131638-C-A

8615477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9131640-C-T

8615578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9131735-G-A

8615635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9131795-C-G

8615664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9131855-C-T

8615703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9131898-C-G

8615703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9131898-C-T

8615747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9131954-A-T

8615789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9131996-T-A

8616143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9132317-G-C

8616159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9132333-C-G

8616173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9132346-C-T

8616178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9132351-C-T

8616400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9132546-A-T

8616424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9132570-C-T

8616538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9132681-G-A

8616641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9132753-G-T

8616689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9132794-G-A

8616768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9132870-A-G

8616816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9132915-G-A

8616826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9132923-G-C

8616828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9132925-T-G

8616919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9132991-G-A

8616931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9133005-A-G

8616969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9133044-G-T

8618328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9133751-A-G

8618540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9133972-G-C

http://identifiers.org/hco/7/GRCh38#8618618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#9134050-C-A

http://identifiers.org/hco/7/GRCh38#8618984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#9134420-A-C

8618986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9134508-T-A

8618986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9134508-T-G

8618987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9134509-T-G

8618989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9134511-G-A

8618989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9134511-G-T

8619207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9134847-G-A

http://identifiers.org/hco/7/GRCh38#8619361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9134983-C-A

http://identifiers.org/hco/7/GRCh38#8619375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9134997-A-C

8619468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9135087-C-G

8619468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9135087-C-T

8619619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9135241-A-G

8619649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9135275-A-T

8619693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9135314-G-A

http://identifiers.org/hco/7/GRCh38#8620725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9135755-C-A

8620752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9135781-G-A

8620752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9135781-G-T

8620828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9135881-G-A

8620828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9135881-G-C

8620828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9135881-G-T

8620841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9135894-A-G

http://identifiers.org/hco/7/GRCh38#8621072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9136071-A-C

8621091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9136090-G-A

8621099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9136098-A-T

8621142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9136222-C-T

8621309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9136421-C-T

8621336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9136441-G-A

http://identifiers.org/hco/7/GRCh38#8621438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9136537-C-A

8622005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9136839-A-G

8622136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9136972-T-C

8622158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9136986-A-G

8624396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9146208-T-C

8624421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9146236-G-A

8624767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9146685-A-G

8624783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9146737-A-T

8625110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9147303-G-C

8625110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9147303-G-T

8625232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9147423-A-T

8625250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9147441-A-G

8625341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9147539-G-A

8625604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9147785-G-A

8625646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9147826-C-T

8625672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9147852-G-A

http://identifiers.org/hco/7/GRCh38#8625749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9147927-A-C

8625785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9147963-T-C

8625823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9148000-G-A

8625823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9148000-G-C

http://identifiers.org/hco/7/GRCh38#8626149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9148327-C-A

8626188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9148366-T-C

8626190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9148368-T-A

8626190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9148368-T-G

8626401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9148911-G-T

8626487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9148981-T-C

8626487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9148981-T-G

8626719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9149208-A-G

8627043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9149514-C-G

8627245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9149699-G-A

8627290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9149730-A-G

http://identifiers.org/hco/7/GRCh38#8628184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9150629-C-A

8628247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9150690-C-T

8628259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9150702-G-A

8628320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9150766-T-A

8628334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9150780-C-T

http://identifiers.org/hco/7/GRCh38#8628409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9150836-C-A

8628409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9150836-C-T

8628880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9151230-C-G

8628889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9151239-G-A

8629247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9151557-G-A

8629360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9151666-C-G

8629401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9151707-T-A

8629401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9151707-T-C

8629472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9151777-T-C

8629551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9151869-G-T

8629597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9151920-A-G

8629607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9151930-C-T

8630531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9153869-T-A

8632346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9154299-A-G

8632515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9154447-T-C

8632576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9154507-G-A

8632740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9154675-G-A

http://identifiers.org/hco/7/GRCh38#8634707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9156447-C-A

8634707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9156447-C-T

http://identifiers.org/hco/7/GRCh38#8634729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9156468-C-A

8634729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9156468-C-G

8634729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9156468-C-T

8634789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9156528-G-A

8634821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9156558-C-T

8634837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9156574-A-G

8634865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9156583-C-T

http://identifiers.org/hco/7/GRCh38#8635131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9156710-C-A

8635131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9156710-C-T

8635411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9157147-T-C

8635580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9157294-T-C

8635711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9157416-G-A

8635766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9157445-A-G

8635854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9157508-A-G

http://identifiers.org/hco/7/GRCh38#8635950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9157600-C-A

8637177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9158779-G-A

8637185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9158787-C-G

8637185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9158787-C-T

8637690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9158971-C-T

8637838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9159079-A-G

http://identifiers.org/hco/7/GRCh38#8637961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9159156-C-A

8638214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9159406-A-G

http://identifiers.org/hco/7/GRCh38#8638253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9159445-A-C

8638253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9159445-A-G

8638285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9159477-T-G

8638367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9159560-C-G

8638376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9159569-G-A

8639220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9160297-C-T

8639463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9160532-G-A

8640162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9160983-T-C

8640247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9161052-C-T

8640553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9161391-C-T

8640588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9161427-C-T

8640591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9161430-A-G

8640591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9161430-A-T

8640614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9161455-A-T

8640629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9161470-T-C

8640665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9161506-C-G

8641549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9162165-C-T

http://identifiers.org/hco/7/GRCh38#8641562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9162178-A-C

8641742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9162385-C-T

http://identifiers.org/hco/7/GRCh38#8654992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9164262-C-A

8655060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9164327-C-T

8655070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9164337-G-T

8656219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9165146-A-G

8656406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9165331-G-A

http://identifiers.org/hco/7/GRCh38#8656409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9165334-C-A

8656409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9165334-C-T

8657042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9165561-T-G

8657045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9165564-T-C

8657083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9165605-T-C

8657158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9165675-G-A

8657158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9165675-G-C

8657200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9165715-C-G

8657242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9165775-G-A

http://identifiers.org/hco/7/GRCh38#8657284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9165813-A-C

8658047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9165939-A-G

8658651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9166551-C-T

8658671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9166570-G-A

8658697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9166604-T-C

8658825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9166727-A-T

8658962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9170573-G-A

8659088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9170679-T-G

http://identifiers.org/hco/7/GRCh38#8659297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9170880-A-C

8659297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9170880-A-G

8659324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9170900-C-T

8659819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9170992-A-G

8659902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9171060-G-T

8659930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9171088-T-C

8659941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9171097-G-T

8659980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9171136-T-C

8660093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9171241-A-G

8660134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9171274-T-C

8660402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9171483-G-A

8660402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9171483-G-C

8660402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9171483-G-T

8660431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9171514-T-C

8660431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9171514-T-G

8660477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9171559-C-G

8660477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9171559-C-T

8660612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9171715-T-C

8660619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9171722-A-G

8660639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9171742-A-T

8660738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9171842-A-G

http://identifiers.org/hco/7/GRCh38#8660814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9171932-C-A

8660892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9171996-A-G

8660937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9172039-C-T

http://identifiers.org/hco/7/GRCh38#8661052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9172158-C-A

8661093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9172199-A-T

8661269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9172363-G-A

8661269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9172363-G-T

http://identifiers.org/hco/7/GRCh38#8661352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9172439-A-C

8661686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9172594-T-A

8661785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9172686-T-G

8661865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9172761-T-C

8661868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9172764-T-A

8661868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9172764-T-C

8662003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9172897-T-C

8670468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9179235-G-A

http://identifiers.org/hco/7/GRCh38#8670520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9179292-C-A

http://identifiers.org/hco/7/GRCh38#8670531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9179303-C-A

8670539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9179311-T-C

http://identifiers.org/hco/7/GRCh38#8670648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9179412-C-A

8670654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9179418-C-T

http://identifiers.org/hco/7/GRCh38#8670943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9180075-C-A

8670943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9180075-C-T

8670961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9180093-G-A

8671007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9180139-A-T

8671034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9180167-C-G

8671208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9180328-G-A

8671208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9180328-G-C

8671209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9180329-T-A

8671458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9180560-T-A

8671517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9180619-C-G

8672628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9181011-A-G

http://identifiers.org/hco/7/GRCh38#8672721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9181103-A-C

8673096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9181439-T-C

8673211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9181549-A-G

8673236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9181574-G-A

8673236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9181574-G-T

8673353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9181678-G-C

8673406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9181730-A-G

8673520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9181814-G-C

8673637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9181937-A-T

8674673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9182478-A-G

8674673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9182478-A-T

8674681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9182486-C-T

8674852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9182656-G-T

8675228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9183053-T-G

8675796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9183492-A-G

8676211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9184451-G-A

8676211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9184451-G-T

http://identifiers.org/hco/7/GRCh38#8676280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9184524-A-C

8676280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9184524-A-T

8676343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9184583-C-G

8676607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9184868-T-A

8676647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9184908-T-C

8676669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9184929-C-T

8676806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9185055-G-C

8676814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9185063-C-T

8678010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9187643-T-A

8678075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9187702-T-A

8678075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9187702-T-C

8678166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9187790-T-C

8680069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9187887-G-A

8680237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9188042-T-C

8680387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9188171-A-G

http://identifiers.org/hco/7/GRCh38#8680433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9189377-A-C

8680433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9189377-A-G

8680771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9189710-A-G

8680782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9189721-G-A

8680835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9189774-G-A

8680879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9189818-C-T

8680959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9189896-A-G

8680974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9189911-A-G

http://identifiers.org/hco/7/GRCh38#8681065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9190006-C-A

8681431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9190349-A-G

8681447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9190358-T-C

8681596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9190501-T-G

http://identifiers.org/hco/7/GRCh38#8681631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9190535-C-A

8681631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9190535-C-G

8681632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9190536-A-T

8681774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9190659-C-T

8681781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9190666-C-T

http://identifiers.org/hco/7/GRCh38#8681808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9190690-C-A

8681825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9190706-T-A

8682191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9191047-G-A

8682291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9191266-A-G

8682379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9191326-A-T

8682468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9191410-G-A

8682468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9191410-G-T

8682497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9191434-C-T

8682624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9191502-A-T

8682714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9191589-T-C

8682829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9191704-A-G

8682839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9191714-G-A

http://identifiers.org/hco/7/GRCh38#8683795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9193487-C-A

8683795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9193487-C-T

8683812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9193504-T-C

8683813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9193505-G-A

8683814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9193506-A-G

8684137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9193793-A-T

8684156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9193812-G-A

8684198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9193869-G-A

http://identifiers.org/hco/7/GRCh38#8684421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9194078-A-C

8684617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9194268-G-A

8685146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9194961-T-G

http://identifiers.org/hco/7/GRCh38#8685163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9194978-A-C

8685163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9194978-A-G

8686100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9195139-C-G

8686491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9195525-T-C

8686517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9195551-G-C

8686708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9195740-T-C

8686829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9195856-G-T

8686858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9195875-G-A

8686910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9195927-C-T

8687022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9196030-A-G

8687275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9196249-T-C

8687303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9196280-G-A

8687407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9196376-T-C

8687571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9196548-T-C

http://identifiers.org/hco/7/GRCh38#8687657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9198116-C-A

8687685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9198144-T-A

8687780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9198239-T-C

8687921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9198384-T-C

8688067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9198564-C-G

8688075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9198572-A-T

8688478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9199280-G-A

8688561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9199351-T-C

http://identifiers.org/hco/7/GRCh38#8688613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9199394-C-A

8688667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9199439-A-G

8688696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9199471-G-A

8688867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9199635-T-A

8688939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9199704-T-C

8688981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9199745-C-G

8689037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9199906-A-G

8689314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9200244-A-G

http://identifiers.org/hco/7/GRCh38#8689340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9200272-C-A

8689340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9200272-C-T

8689415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9200334-G-C

8689415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9200334-G-T

http://identifiers.org/hco/7/GRCh38#8689484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9200378-C-A

http://identifiers.org/hco/7/GRCh38#8689486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9200380-C-A

8689486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9200380-C-T

8689606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9200496-C-G

8689616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9200506-G-A

8689632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9200521-G-T

8689665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9200554-C-G

8689685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9200562-G-C

8690079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9200941-G-A

8690227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron variant
orthologous variants: 9201091-G-T

8690345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 9201210-G-C

8690345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 9201210-G-T

8690535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9201394-A-G

8690735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9201615-A-G

8691101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9201965-G-A

8691990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9202290-G-A

8692093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9202367-A-G

8692270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9202546-A-G

8692579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9202982-C-G

8692579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9202982-C-T

http://identifiers.org/hco/7/GRCh38#8692623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9203028-C-A

8692623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9203028-C-T

8692651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9203056-T-C

8692693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9203098-T-A

8692752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9203155-G-A

8692776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9203179-T-C

8692957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9203354-G-A

8692957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9203354-G-C

8692957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9203354-G-T

8693052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9203443-T-G

8693077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9203468-G-A

8693201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9203551-A-G

http://identifiers.org/hco/7/GRCh38#8693266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9203615-C-A

8693409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9203686-G-A

8693467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9203740-C-T

8693469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9203742-G-T

8693487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9203760-T-C

8693823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9204068-G-C

8693870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9204116-G-C

8693870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9204116-G-T

8693941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9204182-A-G

8693947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9204188-T-C

8694083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9204324-T-C

8694083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9204324-T-G

8694528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9204756-A-G

8694698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9204842-C-T

8694726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9204874-A-G

http://identifiers.org/hco/7/GRCh38#8695177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9205280-A-C

8695522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9205451-T-C

8695522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9205451-T-G

8695581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9205503-A-T

http://identifiers.org/hco/7/GRCh38#8695601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9205524-C-A

8695601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9205524-C-G

http://identifiers.org/hco/7/GRCh38#8695792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9205689-A-C

8695796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9205693-A-G

http://identifiers.org/hco/7/GRCh38#8695909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9205792-A-C

8695983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9205855-G-A

8696054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9205935-G-A

8696096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9205980-G-T

8696184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9206078-G-A

8696218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9206111-T-A

8696364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9206243-G-A

8696414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9206278-C-G

8696414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9206278-C-T

8696509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9206377-G-A

8696509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9206377-G-T

8696654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9206516-T-G

8696682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9206541-A-T

http://identifiers.org/hco/7/GRCh38#8697173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9206562-A-C

8697176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9206565-A-G

8697363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9206736-T-C

8697511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9206886-C-T

8697656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9206965-G-A

8697656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9206965-G-C

8697656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9206965-G-T

8697747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9207042-G-A

8697754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9207049-A-T

8697823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9207114-A-G

8697845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9207136-C-G

8697925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9207207-T-G

8698018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9207294-T-C

8698031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9207309-A-T

http://identifiers.org/hco/7/GRCh38#8698155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9207421-C-A

8698175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9207441-T-C

8698204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9207468-C-T

8698224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9207477-A-G

8698660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9207807-T-C

8698863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9207982-T-G

8699335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9208417-A-G

8699529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9208603-A-G

8699717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9208797-C-T

8699718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9208798-G-A

8699718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9208798-G-T

http://identifiers.org/hco/7/GRCh38#8700116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9209165-A-C

8700144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9209191-G-C

8700231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9209257-G-T

http://identifiers.org/hco/7/GRCh38#8700484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9209478-C-A

8700484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9209478-C-T

8700502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9209495-C-T

8700513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9209506-T-C

8700533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9209526-G-T

http://identifiers.org/hco/7/GRCh38#8700606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9209761-C-A

8700606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9209761-C-G

8700836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9210377-G-C

8700843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9210388-G-A

8700994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9210525-G-A

http://identifiers.org/hco/7/GRCh38#8701264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9210736-A-C

8701274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9210746-T-C

8701671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9211144-T-C

8702034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9211508-T-A

8702206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9211677-C-T

8702454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9211782-G-C

8702454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9211782-G-T

8702465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9211792-C-T

8702476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9211803-C-T

8702478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9211805-T-C

8702659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9211973-A-G

8702712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9212025-T-A

8703038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9212346-G-A

8703107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9212411-G-C

8703153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9212453-C-G

8703185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9212484-G-C

8703197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9212496-C-G

8703321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9212603-T-C

8703567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9212835-T-C

http://identifiers.org/hco/7/GRCh38#8703725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9214856-C-A

8703747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9214875-G-T

8703771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9214894-T-G

8703809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9214930-C-T

8703907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9215002-C-T

8704003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9215105-G-C

8704274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9215322-G-A

8704649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9215678-T-C

8704685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9215716-A-G

8704685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9215716-A-T

8704724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9215758-A-G

8704771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9215800-G-A

http://identifiers.org/hco/7/GRCh38#8704938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9215924-C-A

8705003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9216033-A-G

8705027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9216057-T-A

8705155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9216199-T-C

8705291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9216328-A-G

8705680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9216697-C-T

8705748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9216766-A-G

8705761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9216780-C-G

8705774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9216793-C-T

8705892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9216912-C-T

8706115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9217119-T-C

8706228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9217236-C-T

8706273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9217285-G-A

8706274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9217286-G-A

8706274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9217286-G-T

8706528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9217653-G-A

8706654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9217780-T-C

8706659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9217785-A-G

8707075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9218009-G-A

8707075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9218009-G-C

8707314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9218218-T-C

8707510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9218438-A-T

8707537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9218466-T-C

8707697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9218560-T-C

8707880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9218716-T-C

http://identifiers.org/hco/7/GRCh38#8708136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9218980-C-A

8708136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9218980-C-G

8708248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9219090-T-C

8708969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9219965-C-T

http://identifiers.org/hco/7/GRCh38#8709105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9220069-A-C

8709151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9220117-C-T

8709187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9220155-A-G

8709225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9220189-T-G

8709351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9220308-A-G

8709481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9220448-C-G

8709634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9220601-G-T

8709670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9220637-C-T

8710193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9221155-G-C

8710575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9221546-G-A

http://identifiers.org/hco/7/GRCh38#8710633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9221606-C-A

8711052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9221689-A-G

http://identifiers.org/hco/7/GRCh38#8711094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9221725-C-A

8711094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9221725-C-T

8711102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9221733-T-C

8711180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9221811-C-T

8711216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9221839-T-C

8711574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9222243-T-A

8711655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9222321-C-G

8711679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9222345-T-A

8712232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9222794-T-C

8712462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9223031-A-G

8712478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9223047-A-G

8712669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9223243-C-G

8712669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9223243-C-T

8712671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9223245-C-T

http://identifiers.org/hco/7/GRCh38#8712680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9223254-C-A

8712691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9223265-C-G

8712704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9223278-T-C

8712713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9223287-T-A

8715871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9223688-G-C

8716238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9224116-T-C

8716590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9224382-A-G

8716596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9224388-G-C

8716673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9224451-T-C

8716718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9224507-A-T

8716867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9224614-G-T

8717115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9224828-C-T

8717118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9224831-T-C

8717205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9224910-T-C

8717647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9225918-T-A

8717662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9225935-A-G

8717666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9225939-G-T

http://identifiers.org/hco/7/GRCh38#8717822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9226116-C-A

8717913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9226187-C-T

http://identifiers.org/hco/7/GRCh38#8717925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9226198-A-C

8717963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9226234-C-T

8717996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9226267-G-A

8718013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9226283-C-T

8718124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9226398-T-G

8718608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9226899-G-A

8719087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9227347-C-G

8719355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9227609-A-G

8719463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9227715-T-G

8719482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9227734-A-T

http://identifiers.org/hco/7/GRCh38#8719789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9228051-A-C

http://identifiers.org/hco/7/GRCh38#8719982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9228758-C-A

8720115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9228889-G-C

8720555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9230670-G-T

8720886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9231002-G-T

8720967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9231069-G-C

8720993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9231096-G-A

8721032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9231134-A-G

8721077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9231179-T-C

8721137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9231239-G-A

8721144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9231248-T-A

8721499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9231598-T-A

8721499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9231598-T-G

http://identifiers.org/hco/7/GRCh38#8721829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9231645-A-C

8722010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9231805-G-C

http://identifiers.org/hco/7/GRCh38#8722046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9231841-C-A

8722050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9231845-C-G

8722050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9231845-C-T

8722215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9232577-T-C

http://identifiers.org/hco/7/GRCh38#8722251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9232618-A-C

8722261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9232628-A-T

8722336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9232710-T-C

8722433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9232805-C-T

8722449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9232834-C-T

8722500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9232872-A-G

8722573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9232944-T-C

8723465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9233831-C-T

8724261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9234968-A-G

http://identifiers.org/hco/7/GRCh38#8724282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#9234989-A-C

8724561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9235204-T-C

8724818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9235454-G-A

8724872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9235505-G-A

8724872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9235505-G-C

8724888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9235521-C-T

8725598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9235879-T-G

http://identifiers.org/hco/7/GRCh38#8725625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9235905-C-A

8725841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9236121-T-A

8732477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9237185-C-G

8732477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9237185-C-T

8732615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9237325-G-A

http://identifiers.org/hco/7/GRCh38#8732629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9237339-A-C

8732629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9237339-A-G

8740045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9238090-C-G

8740045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9238090-C-T

8740090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9238136-G-A

8740094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9238140-G-A

8740094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9238140-G-C

8740135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9238180-A-G

8740477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9238486-C-G

8740936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9239158-T-A

8741040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9239247-C-T

8741309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9239466-T-C

http://identifiers.org/hco/7/GRCh38#8741341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9239496-A-C

8741672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9239783-A-G

8741733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9239842-T-C

8741734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9239843-A-G

8742170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9240203-G-C

8742202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9240235-T-A

8742202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9240235-T-C

8742295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9240335-G-A

8742295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9240335-G-T

8743193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9240664-A-T

http://identifiers.org/hco/7/GRCh38#8743245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9240759-A-C

8743245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9240759-A-T

8745143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9242032-C-T

8745176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9242059-A-G

8745182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9242072-C-G

8745323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9242244-G-C

8745323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9242244-G-T

8745383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9242290-G-A

8745384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9242291-T-C

8745398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9242304-G-C

8745441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9242348-G-A

8745441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9242348-G-T

8745450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9242358-G-T

8746005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9242651-A-T

8746070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9242705-G-A

8746146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9242785-C-T

8746216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9242857-G-T

8746397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9243027-T-G

8746439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9243063-A-G

8746490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9243114-T-G

8746501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9243125-T-C

8746642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9243256-G-A

8746642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9243256-G-T

8746718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9243326-C-G

8746852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9243452-C-T

8746896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9243493-G-A

8746896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9243493-G-T

8746905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9243502-G-C

8747483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9244036-T-C

8747720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9244256-C-G

8747720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9244256-C-T

8748057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9244711-G-A

8748079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9244725-T-C

8748098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9244744-C-T

8748130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9244771-T-C

8748318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9244919-A-G

8748321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9244922-G-C

8748424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9245034-G-A

8748669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9245287-A-G

8748696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9245314-C-G

8748739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9245406-G-A

8748938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9245570-G-A

8748996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9245623-G-A

8749658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9246016-G-C

8749716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9246039-T-G

8749734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9246057-T-A

8749734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9246057-T-C

8749974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9246254-T-C

http://identifiers.org/hco/7/GRCh38#8750095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9246394-A-C

8750133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9246432-A-G

8750133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9246432-A-T

8750150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9246449-T-C

8750237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9246574-C-G

8750251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9246588-C-G

8750251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9246588-C-T

8750503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9246648-G-T

8750580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9246723-A-G

8750616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9246761-G-T

8750806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9246952-G-T

8750905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9246977-T-A

8750905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9246977-T-C

8750905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9246977-T-G

http://identifiers.org/hco/7/GRCh38#8750926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9246998-C-A

8750926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9246998-C-G

8750926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9246998-C-T

8750975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9247046-G-C

8750975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9247046-G-T

http://identifiers.org/hco/7/GRCh38#8751277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#9247354-C-A

8751277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 9247354-C-G

8751631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 9247708-T-C

8751631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9247708-T-G

http://identifiers.org/hco/7/GRCh38#8751800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#9247876-A-C

8751800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9247876-A-T

8751805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9247881-T-C

8751815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9247891-T-C

8751862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9247938-G-C

8751862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20693
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9247938-G-T