http://identifiers.org/hco/10/GRCh38#8045387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#9892537-A-C

8045422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5 prime UTR variant
orthologous variants: 9892505-T-A

8045422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5 prime UTR variant
orthologous variants: 9892505-T-C

8045422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5 prime UTR variant
orthologous variants: 9892505-T-G

8045572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9892345-C-T

8045767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9892151-T-C

http://identifiers.org/hco/10/GRCh38#8045798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#9892119-C-A

8045798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9892119-C-T

http://identifiers.org/hco/10/GRCh38#8045819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#9892094-C-A

8045995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9891911-T-C

8046055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9891850-G-T

8046137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9891769-C-T

8046152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9891755-A-G

8046326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9891519-G-A

8046889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9891044-T-A

8046983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9890955-T-A

8047015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9890917-T-A

8047143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9890795-G-T

8047359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9890598-C-T

8047616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9890346-G-A

http://identifiers.org/hco/10/GRCh38#8047636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#9890320-A-C

8047792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9890161-C-T

8047813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9890137-G-A

8047813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9890137-G-C

http://identifiers.org/hco/10/GRCh38#8047814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9890136-C-A

http://identifiers.org/hco/10/GRCh38#8047959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9889983-A-C

8048121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9889822-A-G

8048205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9889728-G-A

http://identifiers.org/hco/10/GRCh38#8048493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9889481-C-A

http://identifiers.org/hco/10/GRCh38#8048557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9889419-A-C

8048723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9889323-C-T

8048811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9889235-C-T

http://identifiers.org/hco/10/GRCh38#8048841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9889205-C-A

8048968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9889076-G-C

http://identifiers.org/hco/10/GRCh38#8049005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9889032-C-A

http://identifiers.org/hco/10/GRCh38#8049407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9888659-C-A

http://identifiers.org/hco/10/GRCh38#8049454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9888614-C-A

8049454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9888614-C-G

8049538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9888521-G-T

8049632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9888424-C-T

8049724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9888331-C-G

8049816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9888243-C-T

8050156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9887926-A-G

8050203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9887879-G-T

8050331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9887753-T-C

8050913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9887161-A-G

8050987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9887068-G-T

8050996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9887059-G-A

8050996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9887059-G-T

8051013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9887045-G-A

8051013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9887045-G-T

8051036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9887022-A-G

8051150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9886909-G-A

8051162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9886897-G-A

8051162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9886897-G-C

8051162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9886897-G-T

http://identifiers.org/hco/10/GRCh38#8051213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#9886807-C-A

8051213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9886807-C-T

8051388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9886646-G-A

8051388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9886646-G-T

8051443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9886599-C-T

8051583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 9886458-G-T

8051631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9886399-G-A

8051631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9886399-G-T

8051663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9886367-G-T

http://identifiers.org/hco/10/GRCh38#8051704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#9886324-C-A

8051704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9886324-C-T

8051708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9886321-G-T

8051757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9886277-T-C

8051757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9886277-T-G

http://identifiers.org/hco/10/GRCh38#8052177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#9885856-C-A

8052177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9885856-C-G

8052177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9885856-C-T

8052309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9885731-T-G

8052331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9885711-A-G

8052390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9885649-G-A

8052390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9885649-G-C

8052390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9885649-G-T

8052404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9885632-C-G

8052501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9885502-G-T

8052520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9885483-G-A

8052520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9885483-G-T

8052541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9885455-G-A

8052541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9885455-G-T

8052911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9885084-G-A

8052911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9885084-G-C

8052911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9885084-G-T

http://identifiers.org/hco/10/GRCh38#8052916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#9885079-C-A

8052916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9885079-C-G

8052916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9885079-C-T

http://identifiers.org/hco/10/GRCh38#8052985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#9885016-C-A

8052985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9885016-C-G

8052985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9885016-C-T

8053255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9884751-G-A

8053255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9884751-G-T

8053416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9884628-G-A

8053416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9884628-G-C

8053416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9884628-G-T

8053422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9884622-G-A

8053422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9884622-G-T

8053446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9884598-C-T

8053571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9884469-G-T

8053605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9884436-G-T

http://identifiers.org/hco/10/GRCh38#8053634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9884408-C-A

8053634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9884408-C-G

8053634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9884408-C-T

http://identifiers.org/hco/10/GRCh38#8053656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9884386-C-A

8053656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9884386-C-T

http://identifiers.org/hco/10/GRCh38#8053671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9884371-C-A

8053671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9884371-C-T

8053736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9884309-A-G

8053749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9884296-T-A

8053817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9884242-G-A

http://identifiers.org/hco/10/GRCh38#8053821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9884238-C-A

8053821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9884238-C-T

8053871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9884200-G-A

8053871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9884200-G-T

http://identifiers.org/hco/10/GRCh38#8053901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9884175-C-A

8053901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9884175-C-T

8053910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9884166-T-C

8054110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9883987-A-G

8054440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9883670-G-A

8054646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9883441-C-T

8054801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9883299-G-A

8054801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9883299-G-C

8054801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9883299-G-T

http://identifiers.org/hco/10/GRCh38#8054958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9883114-A-C

8054958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9883114-A-G

8054958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9883114-A-T

8055030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9883036-G-A

8055037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9883029-C-G

8055037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9883029-C-T

8055118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9882977-G-C

8055169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9882926-T-C

8055190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9882905-G-A

8055210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9882885-G-A

8055210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9882885-G-T

http://identifiers.org/hco/10/GRCh38#8055308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9882774-C-A

http://identifiers.org/hco/10/GRCh38#8055372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9882720-C-A

8055372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5 prime UTR variant
orthologous variants: 9882720-C-G

8055395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5 prime UTR variant
orthologous variants: 9882688-T-A

8055395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5 prime UTR variant
orthologous variants: 9882688-T-C

8055395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5 prime UTR variant
orthologous variants: 9882688-T-G

8055417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5 prime UTR variant
orthologous variants: 9882654-T-C

8055417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5 prime UTR variant
orthologous variants: 9882654-T-G

8055418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5 prime UTR variant
orthologous variants: 9882653-G-T

8055426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5 prime UTR variant
orthologous variants: 9882627-G-T

http://identifiers.org/hco/10/GRCh38#8055480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9882567-C-A

8055480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5 prime UTR variant
orthologous variants: 9882567-C-T

http://identifiers.org/hco/10/GRCh38#8055481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9882566-C-A

http://identifiers.org/hco/10/GRCh38#8055643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9882411-C-A

8055643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 5 prime UTR variant
orthologous variants: 9882411-C-T

http://identifiers.org/hco/10/GRCh38#8055836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9882221-C-A

8055836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: missense variant
orthologous variants: 9882221-C-G

8055836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: missense variant
orthologous variants: 9882221-C-T

8055957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9882101-G-A

8056029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9882033-A-G

http://identifiers.org/hco/10/GRCh38#8056102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9881939-C-A

8056103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9881938-A-G

8056331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9881733-C-T

http://identifiers.org/hco/10/GRCh38#8056337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9881727-A-C

http://identifiers.org/hco/10/GRCh38#8056456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9881626-C-A

http://identifiers.org/hco/10/GRCh38#8056634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9881453-C-A

8056959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9881083-G-A

8056989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9881053-C-T

8057273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9880749-G-C

http://identifiers.org/hco/10/GRCh38#8057581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9880442-A-C

8057811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9880247-G-A

8057904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9880155-T-C

8057976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9880084-G-A

8057976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9880084-G-C

http://identifiers.org/hco/10/GRCh38#8058020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9880040-C-A

8058020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9880040-C-T

http://identifiers.org/hco/10/GRCh38#8058243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9879827-C-A

8058243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9879827-C-T

http://identifiers.org/hco/10/GRCh38#8058269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9879783-C-A

8058329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: missense variant
orthologous variants: 9879710-T-G

8058391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: missense variant
orthologous variants: 9879648-T-C

8058430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: missense variant
orthologous variants: 9879609-C-T

http://identifiers.org/hco/10/GRCh38#8058517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9879522-A-C

8058523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: missense variant
orthologous variants: 9879516-C-T

8058527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: missense variant
orthologous variants: 9879512-C-T

http://identifiers.org/hco/10/GRCh38#8058529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9879510-A-C

8058529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: missense variant
orthologous variants: 9879510-A-G

8058664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: missense variant
orthologous variants: 9879375-T-A

8058875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9879164-C-T

8058928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9879088-G-A

8058928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9879088-G-T

8058990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9879034-G-A

8058990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9879034-G-T

8059455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9878534-G-A

8059455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9878534-G-C

http://identifiers.org/hco/10/GRCh38#8059464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9878525-A-C

8059479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9878511-A-G

8059603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9878406-C-T

8059607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9878402-A-G

8060494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9877524-C-G

8060714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9877325-G-A

8060955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9877076-G-A

8061548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9876421-G-A

8061932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9876004-C-T

8061977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9875965-A-T

8061981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9875961-G-A

8062035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9875891-G-A

8062035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9875891-G-T

8062330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9875605-G-A

http://identifiers.org/hco/10/GRCh38#8062335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9875600-A-C

8062434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9875520-G-A

8062575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9875353-G-T

8062709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9875129-G-A

8062779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9875044-A-G

8062791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9875032-T-A

8062791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9875032-T-C

8063069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9874781-G-T

8063163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9874680-C-T

8063420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9874367-C-T

8063610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9874175-A-G

8063611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9874174-T-G

8063620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9874165-T-G

8063936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9873771-T-C

8064275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9873458-T-A

8064275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9873458-T-C

8064881-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9872784-T-A

8064992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9872660-G-T

8065133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9872524-T-C

8065190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9872477-C-G

8065667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9872306-T-C

8065861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9872118-G-A

8065861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9872118-G-T

http://identifiers.org/hco/10/GRCh38#8065920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#9872068-C-A

8065998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9872014-G-A

8066103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9871930-G-A

http://identifiers.org/hco/10/GRCh38#8066127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9871910-A-C

8066127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9871910-A-G

8066261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9871796-A-T

8066351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9871705-C-G

8066463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9871389-A-T

8066471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9871381-G-C

8066471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9871381-G-T

8066472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9871380-A-G

8066472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9871380-A-T

8066562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9871272-G-T

8067050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9870786-A-G

8067050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9870786-A-T

8067485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9870377-C-T

8068045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9869977-A-G

8068077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9869954-A-G

8068093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9869938-A-G

8068260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9869351-T-C

8068959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9868540-T-C

8069014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9868484-G-C

8069064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9868429-G-A

8069203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9868318-G-A

8069239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9868270-T-C

8069462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9868040-C-G

8069462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9868040-C-T

8069683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9867808-A-G

8069918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9867135-A-G

8069929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9867124-C-T

8070107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9866920-C-T

8070153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9866885-G-A

8070184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9866853-G-A

8070230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9866809-C-T

8070234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9866805-G-T

8070408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9866663-C-T

8070719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9866424-C-T

8070848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9866317-G-A

8071134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron_variant, undefined
orthologous variants: 9866061-T-C

8071191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9866009-A-G

8071398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9865884-G-A

8071499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9865801-A-G

8071543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9865716-G-A

8071559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9865708-C-T

8071570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9865697-C-T

8071658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9865583-G-A

8072012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9865077-C-T

8072055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9865036-G-A

8072094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9865001-T-C

8072105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9864990-C-T

8072259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9864847-A-T

8072260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9864844-G-C

8072260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9864844-G-T

8072335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9864797-G-A

8072342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9864791-G-A

8072458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9864714-A-T

8073231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9864037-C-T

http://identifiers.org/hco/10/GRCh38#8073234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9864034-A-C

8073341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9863928-T-C

8073373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9863894-G-A

8073641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9863546-G-A

8073641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9863546-G-T

http://identifiers.org/hco/10/GRCh38#8073673-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9863526-A-C

8073673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: intron variant
orthologous variants: 9863526-A-G

http://identifiers.org/hco/10/GRCh38#8073946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#9863256-C-A

8073946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 9863256-C-T

8074038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 3 prime UTR variant
orthologous variants: 9863156-C-T

http://identifiers.org/hco/10/GRCh38#8074178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9863009-C-A

8074178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 3 prime UTR variant
orthologous variants: 9863009-C-T

http://identifiers.org/hco/10/GRCh38#8074180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9863007-C-A

8074193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 3 prime UTR variant
orthologous variants: 9862994-G-T

8074448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 3 prime UTR variant
orthologous variants: 9862723-A-G

8074522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 3 prime UTR variant
orthologous variants: 9862606-G-A

8074522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 3 prime UTR variant
orthologous variants: 9862606-G-C

http://identifiers.org/hco/10/GRCh38#8074527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9862601-A-C

8074616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 3 prime UTR variant
orthologous variants: 9862498-T-A

8074616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 3 prime UTR variant
orthologous variants: 9862498-T-C

8074616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 3 prime UTR variant
orthologous variants: 9862498-T-G

8074622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 3 prime UTR variant
orthologous variants: 9862492-T-C

8074622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 3 prime UTR variant
orthologous variants: 9862492-T-G

8074670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 3 prime UTR variant
orthologous variants: 9862451-A-G

8074670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 3 prime UTR variant
orthologous variants: 9862451-A-T

http://identifiers.org/hco/10/GRCh38#8074973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4172
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#9862118-C-A