147390820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454063-T-C

147390975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454236-T-C

147391049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454308-G-C

147391074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454314-A-G

147391102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454341-T-C

147391147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454391-G-T

147391174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454417-T-G

147391187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454429-T-C

http://identifiers.org/hco/5/GRCh38#147391213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43454459-C-A

http://identifiers.org/hco/5/GRCh38#147391257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43454503-C-A

147391257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454503-C-T

147391281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454533-A-T

147391307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454560-T-C

http://identifiers.org/hco/5/GRCh38#147391351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43454620-C-A

147391351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454620-C-T

http://identifiers.org/hco/5/GRCh38#147391358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43454626-C-A

147391359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454627-T-C

147391396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454664-A-G

147391398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454666-G-C

147391427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454697-G-A

147391455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454726-G-A

147391455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454726-G-T

147391469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454736-G-A

147391469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454736-G-T

147391482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454748-T-C

147391482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454748-T-G

147391497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454768-G-A

147391526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454787-C-T

147391556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43454813-T-C

147391782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43455009-T-C

147391833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43455065-T-C

147392007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43455208-C-T

147392480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43455879-C-T

http://identifiers.org/hco/5/GRCh38#147392500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43455899-C-A

147392561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43455960-G-A

147392579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43455979-G-A

147392639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456038-G-A

147392644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456043-G-T

http://identifiers.org/hco/5/GRCh38#147392730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43456132-C-A

http://identifiers.org/hco/5/GRCh38#147392742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43456148-C-A

147392800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456210-G-A

147392800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456210-G-T

147392866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456269-A-G

147392911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456310-T-C

147392947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456345-T-C

http://identifiers.org/hco/5/GRCh38#147393055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43456455-C-A

147393055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456455-C-G

147393126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456502-G-A

147393126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456502-G-C

147393126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456502-G-T

147393139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456515-T-C

147393204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456581-G-A

147393204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456581-G-T

147393229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456606-G-A

147393229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456606-G-T

http://identifiers.org/hco/5/GRCh38#147393257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43456628-C-A

147393291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456659-A-G

147393305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456672-T-C

http://identifiers.org/hco/5/GRCh38#147393342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43456709-C-A

147393371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456733-G-A

147393371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456733-G-T

147393382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456744-G-A

147393382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456744-G-T

147393429-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456789-T-A

147393574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456933-A-G

147393574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456933-A-T

http://identifiers.org/hco/5/GRCh38#147393626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43456985-C-A

147393626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456985-C-T

http://identifiers.org/hco/5/GRCh38#147393638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43456997-C-A

147393638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43456997-C-T

http://identifiers.org/hco/5/GRCh38#147393659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43457017-A-C

http://identifiers.org/hco/5/GRCh38#147393669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43457027-C-A

147393669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43457027-C-T

147393716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43457077-G-A

147393716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43457077-G-C

147393716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43457077-G-T

http://identifiers.org/hco/5/GRCh38#147393730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43457091-C-A

147393730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43457091-C-T

147393731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43457092-A-G

147393811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43457168-G-T

147393812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43457169-G-A

147393812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43457169-G-T

147393969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43457332-G-A

147393969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43457332-G-T

147394074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 43457436-C-T

147394176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43457527-G-A

147394176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43457527-G-T

147394181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43457532-A-G

147394232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43457582-G-A

147394232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43457582-G-T

147394610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43457912-T-C

147394611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43457913-G-C

http://identifiers.org/hco/5/GRCh38#147394693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43457971-A-C

147394693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43457971-A-T

http://identifiers.org/hco/5/GRCh38#147394900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43458181-A-C

147394900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43458181-A-G

147394910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43458191-C-T

147394963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43458244-T-C

147394982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43458259-G-A

147395106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43458372-C-T

147395234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43458462-T-C

147395234-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43458462-T-G

147395292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43458519-C-G

147395308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43458535-T-A

http://identifiers.org/hco/5/GRCh38#147395423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43458651-C-A

147395423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43458651-C-T

147395480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43458708-G-A

147395480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43458708-G-T

147395495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43458723-G-A

147395495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43458723-G-T

147395514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43458742-C-T

147395540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43458771-A-G

147395599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 43458830-T-A

147395724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 43458955-G-T

147395729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 43458960-C-T

147395742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43458971-G-A

http://identifiers.org/hco/5/GRCh38#147395744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43458973-C-A

147395792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43459034-T-C

147395823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43459067-T-C

147396042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43459543-G-T

147396079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43459580-G-T

147396239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43459746-G-A

147396289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43459789-C-T

147396535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43460032-C-G

147396546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43460043-G-A

147396756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43460228-C-T

147396757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43460229-T-C

147397284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43460860-G-A

147397284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43460860-G-C

147397554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43461296-A-G

http://identifiers.org/hco/5/GRCh38#147397594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43461330-C-A

147397614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43461344-G-A

147397614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43461344-G-C

147397614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43461344-G-T

147397643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43461367-C-T

147397647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43461371-G-T

147397747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 43461471-G-A

http://identifiers.org/hco/5/GRCh38#147397804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43461528-C-A

147397804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43461528-C-G

147397851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 43461575-G-T

147397853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 43461577-C-T

http://identifiers.org/hco/5/GRCh38#147397953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43461694-C-A

147397953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43461694-C-T

147397988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43461729-G-A

147397988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43461729-G-T

147398059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43461813-C-T

147398073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43461827-T-C

147398144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43461899-A-G

147398304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43462058-G-A

147398954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43462658-G-A

147398954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43462658-G-T

147399010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43462712-A-G

147399069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43462743-G-A

147399069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43462743-G-C

147399073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43462747-G-A

147399286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43462977-T-C

http://identifiers.org/hco/5/GRCh38#147399319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43463009-C-A

147399319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43463009-C-T

http://identifiers.org/hco/5/GRCh38#147399433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43463093-C-A

147399807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43463628-T-C

147400044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43463864-T-C

147400081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43463884-T-C

147400184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43464986-T-C

147400231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43465031-C-T

147400321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43465118-G-T

147400363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43465160-G-C

http://identifiers.org/hco/5/GRCh38#147400403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43465199-A-C

147400423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43465215-G-A

147400442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43465234-T-A

147400548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43465311-G-C

147400548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43465311-G-T

147400629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43465880-G-A

147400659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43465910-T-A

147400664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43465915-C-G

147400664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43465915-C-T

147400922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43466157-G-A

147400922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43466157-G-T

147401100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43466328-A-G

147401397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43466826-G-A

147401397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43466826-G-C

147401397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43466826-G-T

http://identifiers.org/hco/5/GRCh38#147401433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43466849-C-A

147401443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43466859-T-C

147401443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43466859-T-G

147401506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43466919-C-T

147401724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43467123-G-C

147401724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43467123-G-T

147401873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43467269-G-C

147401873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43467269-G-T

147401893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43467290-G-C

147401893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43467290-G-T

147401984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43467393-A-G

147402011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43467411-T-C

147402086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43467443-C-T

147402176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43467521-T-C

147402277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43467579-T-A

147402289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43467591-G-A

147402325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43467606-T-C

http://identifiers.org/hco/5/GRCh38#147402492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43467758-C-A

147402492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43467758-C-T

147403391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43468469-T-C

http://identifiers.org/hco/5/GRCh38#147403407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43468483-A-C

147403431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43468507-C-G

http://identifiers.org/hco/5/GRCh38#147403945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43473751-C-A

147404159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43473932-C-G

147404328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43474081-G-T

147404521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43474260-G-A

147404522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43474261-C-T

147404634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43474345-G-A

147404965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43474676-G-A

147404999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43474706-C-T

147405160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43474858-T-C

147405488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43475182-G-A

147405488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43475182-G-T

147405523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43475217-C-T

147405525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43475219-C-T

http://identifiers.org/hco/5/GRCh38#147405539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43475233-C-A

147405550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43475245-G-A

147405743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43475440-G-C

147405764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43475459-C-G

147405764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43475459-C-T

http://identifiers.org/hco/5/GRCh38#147405798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43475493-C-A

147405798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43475493-C-G

147405798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43475493-C-T

147405799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43475494-G-A

147405799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43475494-G-C

147405828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43475523-G-T

147405882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43475576-G-T

147405901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43475588-G-A

147405901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43475588-G-T

147405929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43475616-T-C

http://identifiers.org/hco/5/GRCh38#147405948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43475635-A-C

147405963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43475650-A-G

147406033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43475710-G-T

147406038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43475715-A-G

147406205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43475864-G-A

147406226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43475885-C-T

147406236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43475895-T-A

147406333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43475993-A-G

147406339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43475999-T-G

147406344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43476004-A-T

147406499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43476143-G-A

147406701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43476297-C-G

147407370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43476916-G-A

147408038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43477527-T-C

147408066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43477543-C-T

147408404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43477808-C-T

147408623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43478042-T-C

147408656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43478085-C-T

147408916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43478376-T-A

147409007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43478451-A-G

147409096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43478528-G-A

147409203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43478630-G-C

147409363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43478769-T-C

147409509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43478922-G-A

147409563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43478969-T-C

147409708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43479092-C-T

147409787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43479151-T-C

147410846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43481567-C-T

147410918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43481640-A-G

http://identifiers.org/hco/5/GRCh38#147411184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43481896-A-C

147412458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43486792-A-G

147412497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43486832-G-A

147412497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43486832-G-T

http://identifiers.org/hco/5/GRCh38#147412576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43486920-A-C

http://identifiers.org/hco/5/GRCh38#147412597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43486935-C-A

http://identifiers.org/hco/5/GRCh38#147413492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43487702-C-A

147413492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43487702-C-T

http://identifiers.org/hco/5/GRCh38#147413528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43487739-C-A

147413528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43487739-C-T

147413532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43487743-G-A

147413532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43487743-G-T

147413533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43487744-G-A

147413533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43487744-G-T

147413559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43487770-C-T

147413578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43487789-T-C

147413578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43487789-T-G

147413856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43488075-C-T

http://identifiers.org/hco/5/GRCh38#147414010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43488221-C-A

147414010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43488221-C-T

147414369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43489673-C-G

147414686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43489962-C-T

147415069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43490120-G-A

147415069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43490120-G-C

147415096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43490147-G-A

147415154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43490195-T-C

147415511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43491084-G-A

147415511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43491084-G-C

http://identifiers.org/hco/5/GRCh38#147415586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43491174-C-A

147415586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43491174-C-T

147415606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43491194-C-T

147415607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43491195-C-T

147415617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43491205-G-A

147415617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43491205-G-T

147415641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43491228-T-A

147415641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43491228-T-C

147415641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43491228-T-G

147415644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43491236-A-G

147415644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43491236-A-T

147415646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43491238-G-T

147415689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43491279-G-A

147415866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43491456-A-G

147416385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43491831-T-C

147416693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43492622-C-T

147416934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43492872-T-C

147417203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43493147-T-C

147417635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43493546-C-T

147417770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43493673-A-G

147417981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43493758-T-C

147417999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43493776-C-T

147418031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43493808-C-T

147418078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43493824-G-C

147418322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43493908-A-G

147418407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43494000-A-G

http://identifiers.org/hco/5/GRCh38#147418419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43494012-C-A

147418420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43494013-A-G

147418443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43494023-T-A

147418443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43494023-T-G

147418547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43494127-A-G

147418571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43494151-C-G

147418577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43494157-A-T

147418604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43494184-A-G

http://identifiers.org/hco/5/GRCh38#147418786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43494278-A-C

147418831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43494321-T-C

147419003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43494477-T-C

147419014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43494488-T-C

147419036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43494510-A-G

147419114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43494565-C-T

147419246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43494690-C-T

147419479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43494889-T-A

147419629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43495039-A-G

147419840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43495232-C-T

147419944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43495330-T-C

147420033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43495441-G-A

147420308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43495723-T-C

147420504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43495890-G-A

147420504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43495890-G-C

147424273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43496029-A-G

147424294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43496050-T-C

147424294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43496050-T-G

147424834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43496534-G-A

147424834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43496534-G-C

147424834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43496534-G-T

http://identifiers.org/hco/5/GRCh38#147424841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43496541-C-A

147424841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43496541-C-T

147424855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43496548-G-A

147424855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43496548-G-T

147425035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43496724-C-T

147425045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43496734-T-C

147425095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43496784-A-G

http://identifiers.org/hco/5/GRCh38#147425101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43496790-C-A

147425101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43496790-C-T

http://identifiers.org/hco/5/GRCh38#147425103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43496792-C-A

147425117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43496806-G-C

147425136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43496825-C-T

147425550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43497127-T-C

147425738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43497288-G-A

147425827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43497370-T-G

147426026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43497566-C-T

147426280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43497864-G-A

147426394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43497977-G-C

147426394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43497977-G-T

147426529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43498115-C-G

147426740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43498301-C-T

147427052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43498618-T-C

147427078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43498642-C-G

147427078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43498642-C-T

147427139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43498695-C-G

147427206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43498754-A-G

147427239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43498787-T-C

147427239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43498787-T-G

147427402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43498924-T-C

http://identifiers.org/hco/5/GRCh38#147427699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43499391-C-A

147427699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43499391-C-T

147427700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43499392-C-G

147427804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43499471-A-G

147428249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43499857-G-A

147428433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43500057-C-T

147428494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43500115-G-C

147428608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43500225-A-G

147428641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43500258-A-G

147429189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43500791-A-G

147429295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43500874-T-C

147429447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501080-T-A

147429447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501080-T-G

http://identifiers.org/hco/5/GRCh38#147429473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43501169-A-C

147429475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501171-T-C

147429479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501175-C-T

http://identifiers.org/hco/5/GRCh38#147429541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43501239-C-A

147429703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501413-C-G

147429974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501676-T-C

147430166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501856-T-A

147430166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501856-T-G

147430168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501858-G-A

147430168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501858-G-C

http://identifiers.org/hco/5/GRCh38#147430749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43501973-A-C

147430749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501973-A-T

147431378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43502732-T-C

147431403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43502757-G-A

147431778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43503093-G-A

147432055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43503371-C-T

147432158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43503467-C-T

147432195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43503504-G-A

147432634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43503933-G-A

147432635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43503934-A-G

147432675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43503967-G-A

147432855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43504093-G-A

147432855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43504093-G-T

147432890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43504126-A-T

147433228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43504885-G-A

http://identifiers.org/hco/5/GRCh38#147433288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43504945-C-A

147433312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43504967-G-A

147433439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43505077-T-C

147434622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43506718-A-G

http://identifiers.org/hco/5/GRCh38#147434688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43506785-A-C

147434723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43506810-T-G

147434859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43506909-G-T

147435010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43506984-T-A

http://identifiers.org/hco/5/GRCh38#147435751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43507661-C-A

147435751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43507661-C-T

147435760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43507669-T-C

http://identifiers.org/hco/5/GRCh38#147435998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43507920-C-A

147436021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43507943-C-T

147436280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43508203-T-A

147436281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43508204-G-A

147436609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43508983-G-A

147436896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43509243-G-A

147437016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43509352-G-A

147437122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43509440-G-A

147437143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43509462-G-A

147437181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43509500-T-C

147437209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43509528-G-A

147437209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43509528-G-C

147437295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43509614-T-C

147437549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43509868-C-T

147437898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43510198-A-G

147437964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43510261-G-C

147438169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43511237-T-C

147438172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43511240-G-C

147438196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43511263-G-A

147438196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43511263-G-C

147438496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43511510-T-C

147438503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43511515-T-C

147438588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43511599-C-T

147438645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43511652-A-G

147438779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43511786-G-A

147438970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43511937-T-C

http://identifiers.org/hco/5/GRCh38#147439106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43512274-C-A

147439106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43512274-C-T

147439271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43512434-A-G

147439369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43512526-T-G

147439406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43512578-T-C

147439555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43512704-T-C

147439585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43512734-G-C

147439643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43512789-G-A

147439702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43512837-G-A

http://identifiers.org/hco/5/GRCh38#147440533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43513201-A-C

147440581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43513249-A-G

147440834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43513460-G-C

147440914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43513538-T-G

147441129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43513663-C-T

http://identifiers.org/hco/5/GRCh38#147441153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43513686-C-A

147441337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43513812-A-T

147441634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43514088-G-A

147441697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43514133-G-A

147441853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43514272-T-C

147442215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43514597-A-G

http://identifiers.org/hco/5/GRCh38#147442355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43514734-C-A

147442355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43514734-C-T

147442370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43514749-T-A

147442453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43514828-G-A

147442482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43514860-A-G

147442784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43515159-G-C

147443755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43515749-G-A

147443916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43515888-A-G

147444243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43516586-G-C

147444250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43516595-T-C

147444269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43516640-C-G

http://identifiers.org/hco/5/GRCh38#147444719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43517846-C-A

147444751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43517878-T-A

147444751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43517878-T-C

147444795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43517923-G-A

147444893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43518021-G-A

147445514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43518666-A-G

147445716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43518843-G-A

147445775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43518900-G-A

147445940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43519065-T-G

147446117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43519219-C-T

147446198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43519300-C-T

147446453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43519596-G-T

147446560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43519700-G-A

147446561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43519701-G-A

147446605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43519731-C-T

147446606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43519732-A-G

147446955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43520084-T-C

147447147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43520274-T-C

147447225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43520373-A-T

http://identifiers.org/hco/5/GRCh38#147447250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43520397-A-C

147447345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43520482-T-C

147447979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43520798-C-T

147448044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43520862-T-C

147448368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43521143-A-G

147448608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43521371-C-G

147448612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43521375-C-G

147448935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43521701-G-T

http://identifiers.org/hco/5/GRCh38#147449460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43522190-A-C

147449655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43522432-G-A

147449680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43522454-C-G

147449782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43522545-T-C

147449876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43522650-A-G

147450359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43523021-C-T

147450383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43523044-T-A

147450651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43523295-A-G

147451298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43523938-T-C

147451385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43524024-C-T

147451464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43524103-T-C

147451560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43524204-T-C

147451678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43524343-G-C

147451690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43524355-T-C

http://identifiers.org/hco/5/GRCh38#147451929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43524553-A-C

147451930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43524554-C-T

147451971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43524595-G-A

http://identifiers.org/hco/5/GRCh38#147452016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43524639-C-A

http://identifiers.org/hco/5/GRCh38#147452025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43524648-C-A

147452042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43524665-C-G

147452641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43525247-G-T

147452732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43525328-T-C

147452938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43525486-C-T

147453083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43525621-G-A

147453083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43525621-G-T

147453251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43525787-C-T

147453389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43525913-C-T

147453508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43526036-G-A

147453508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43526036-G-T

147453689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43526189-G-T

147453695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43526195-T-A

147453695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43526195-T-G

http://identifiers.org/hco/5/GRCh38#147453734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43526235-C-A

147453734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43526235-C-G

147453734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43526235-C-T

147453740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43526241-G-A

147453740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43526241-G-T

147453853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43526378-T-C

147454088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, undefined
orthologous variants: 43526628-G-A

147454088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, undefined
orthologous variants: 43526628-G-T

147454151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43526695-G-A

147454151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43526695-G-T

http://identifiers.org/hco/5/GRCh38#147454167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43526711-C-A

147454167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43526711-C-T

147454214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43526758-C-T

147454240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43526784-A-G

147454240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43526784-A-T

147454248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43526791-G-A

147454248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43526791-G-T

147454406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43526955-A-G

http://identifiers.org/hco/5/GRCh38#147454481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43527027-C-A

147455215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43527705-G-C

147455230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43527719-C-T

147455461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, undefined
orthologous variants: 43527940-G-T

147455463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, undefined
orthologous variants: 43527942-A-G

147455530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43528022-C-T

147455541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43528033-G-C

http://identifiers.org/hco/5/GRCh38#147455640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43528165-C-A

147455713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43528251-C-T

http://identifiers.org/hco/5/GRCh38#147455786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43528420-C-A

147455786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43528420-C-T

147455893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43528583-T-C

147455893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43528583-T-G

147456160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43528849-C-G

http://identifiers.org/hco/5/GRCh38#147456432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43529132-A-C

147456432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43529132-A-G

147462191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43532595-A-T

147462247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43532651-A-T

147462556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43532881-A-G

http://identifiers.org/hco/5/GRCh38#147462753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43533075-C-A

147462774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43533096-T-C

147462782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43533104-A-G

147462903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43533219-G-C

147463099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43533415-C-T

http://identifiers.org/hco/5/GRCh38#147463510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43533782-A-C

147463522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43533794-G-C

147463654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43533923-A-G

147463661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43533930-G-A

147464020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43534286-C-T

147464028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43534294-A-G

147464028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43534294-A-T

http://identifiers.org/hco/5/GRCh38#147464430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43534625-C-A

147464709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43535000-A-G

147464760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43535039-G-A

147464783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43535062-G-A

147464848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43535125-C-T

147465634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43535316-G-A

147465634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43535316-G-C

http://identifiers.org/hco/5/GRCh38#147465866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43535519-C-A

147465882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43535542-C-T

http://identifiers.org/hco/5/GRCh38#147465912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43535572-C-A

147465987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43535643-G-A

147466549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43536280-G-T

147466820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43536538-G-A

147466866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43536587-A-G

147467019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43536733-C-T

147467236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43536931-A-G

147467318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43537009-A-G

147467319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43537010-T-A

147467402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43537112-T-C

147467427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43537169-A-G

http://identifiers.org/hco/5/GRCh38#147467450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43537226-C-A

147467649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43537660-G-A

147467746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43537755-A-G

147467877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43537880-G-A

147467982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43537975-C-T

147468004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43537998-T-C

147468142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43538135-G-A

147468194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43538233-T-C

147469146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43538628-G-T

147469490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43538962-G-C

147469552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43539023-G-A

147469743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43539189-C-T

147469754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43539205-G-A

147469847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43539280-A-G

147469893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43539328-G-A

147469909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43539344-T-G

http://identifiers.org/hco/5/GRCh38#147470315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43539541-C-A

147470562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43539695-G-A

147470562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43539695-G-T

147470626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43539757-G-T

147470635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43539766-T-C

147470994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43540090-G-A

147471228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43540622-T-G

147471340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43540751-C-G

147471353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43540764-A-G

147471731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43541298-A-G

147471808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43541375-G-A

147472445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43542001-C-T

147472471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43542027-T-C

147472561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron variant
orthologous variants: 43542127-C-T

http://identifiers.org/hco/5/GRCh38#147472679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43542612-C-A

147472712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43542645-T-C

147472721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43542654-T-C

147472757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43542690-A-G

147472775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43542706-G-T

147472917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43542846-C-T

147473099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43543017-T-C

147473356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43543272-G-T

147473394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43543309-T-C

147473426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43543350-G-C

147473437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43543360-G-T

147473473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43543395-G-T

147473550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43543476-G-A

http://identifiers.org/hco/5/GRCh38#147474166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43544171-A-C

147474283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43544282-C-T

147474293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43544292-T-C

147474518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43544503-G-A

147474923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43544902-T-A

147474923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43544902-T-C

147474950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43544928-T-A

147475004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43544982-T-G

147475815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43546954-C-T

147476302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43547470-G-C

147476405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43547570-C-T

http://identifiers.org/hco/5/GRCh38#147476561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43547587-A-C

http://identifiers.org/hco/5/GRCh38#147476610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43547601-A-C

147476610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43547601-A-G

147476938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43547899-T-G

147478029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43550426-T-C

147478245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43550645-C-T

147478342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43550743-T-C

147478382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43550777-G-A

147478394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43550789-T-C

147478509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43550887-T-G

147478516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43550894-C-T

147478536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43550913-G-A

147478771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43551139-G-A

147478771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43551139-G-C

147478974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43551320-A-T

147478975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43551321-G-A

147479017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43551360-T-G

147479260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43551610-G-A

147479295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43551649-T-C

147479701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43552041-C-G

147479929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43552268-A-G

147479936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43552275-T-C

http://identifiers.org/hco/5/GRCh38#147480025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43552361-A-C

147480269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43552562-C-T

147480273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43552566-T-A

147480463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43552728-C-T

147482491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43553314-G-A

147482563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43553395-C-T

http://identifiers.org/hco/5/GRCh38#147482666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43553502-A-C

147483190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43553774-G-A

147483193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43553777-C-T

147483436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43554055-A-G

147483467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43554080-A-G

147483607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43554219-A-G

147483635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43554258-A-G

147484109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43554703-T-C

147484652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43555237-G-A

147484665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43555250-A-T

147484694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43555277-G-A

147484748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43555336-T-C

http://identifiers.org/hco/5/GRCh38#147484754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43555342-A-C

147484757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43555345-A-G

147484874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43555455-T-G

147484985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43555564-C-T

147484997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43555576-G-A

147485316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43556524-C-G

147485404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43556611-C-T

147485609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43556807-G-A

147485940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43557620-G-A

147486092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43557807-C-T

147486373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43558068-T-A

147486373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43558068-T-C

147486970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43558545-T-C

147487167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43558724-G-A

147487816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43559375-C-T

147488205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43559723-A-G

147499345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43561817-T-C

147499472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43561898-A-T

147500240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43562558-T-G

147500250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43562562-G-T

http://identifiers.org/hco/5/GRCh38#147500656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43562906-A-C

147500988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43563207-G-T

147501203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43563412-C-G

147501209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43563418-G-A

147501233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43563442-C-T

147501303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43563604-G-A

147501456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43563770-C-T

147501464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43563778-T-C

147501478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43563793-A-T

147502256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43564437-G-C

147502289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43564468-C-G

147502289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43564468-C-T

147502293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43564472-A-G

147502301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43564480-C-G

147502301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43564480-C-T

147502344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43564523-C-T

147502549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43564878-A-T

http://identifiers.org/hco/5/GRCh38#147503601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43565356-A-C

147503647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43565416-G-A

147503647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43565416-G-T

147503684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43565445-T-C

147503736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43565495-A-G

147503962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43565712-T-A

147503973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43565723-T-G

147504463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43566176-T-C

147504612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43566325-T-C

147504727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43566409-G-A

147504730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43566412-C-G

147504769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43566451-G-A

147505000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43566667-T-C

147505100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43566755-A-G

147505742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43567092-C-T

http://identifiers.org/hco/5/GRCh38#147505847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43567196-A-C

147505938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43567278-G-C

147506036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43567370-G-A

147506343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43567651-G-A

147506386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43567693-T-C

147506551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43567891-G-T

147506577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43567917-C-T

147506704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43568227-T-C

147506704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43568227-T-G

147506863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43568388-T-C

http://identifiers.org/hco/5/GRCh38#147506994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43568511-C-A

147507111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43568629-C-G

http://identifiers.org/hco/5/GRCh38#147507190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43568706-C-A

147507250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43568773-C-T

147507393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43568887-G-T

147507445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43568936-C-T

147507624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43569143-A-G

147507801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43569320-G-A

http://identifiers.org/hco/5/GRCh38#147508280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43569808-A-C

147508554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43570090-G-C

147508736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43570253-C-G

147508905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43570433-T-C

147509111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43570561-G-T

147509372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43570790-C-G

147509372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43570790-C-T

http://identifiers.org/hco/5/GRCh38#147509469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#43570886-C-A

147509469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43570886-C-G

147509469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43570886-C-T

147509556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: synonymous variant
orthologous variants: 43570973-G-A

147509556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: synonymous variant
orthologous variants: 43570973-G-C

147509559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: synonymous variant
orthologous variants: 43570976-G-A

http://identifiers.org/hco/5/GRCh38#147509568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43570985-C-A

147509598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: synonymous variant
orthologous variants: 43571015-G-A

http://identifiers.org/hco/5/GRCh38#147509611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43571025-C-A

147509611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: missense variant
orthologous variants: 43571025-C-G

147509621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: missense variant
orthologous variants: 43571035-C-T

147509626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: missense variant
orthologous variants: 43571040-C-G

147509626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: missense variant
orthologous variants: 43571040-C-T

147509645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: missense variant
orthologous variants: 43571059-C-T

147509739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: synonymous_variant, undefined
orthologous variants: 43571153-G-A

147509739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: missense_variant, undefined
orthologous variants: 43571153-G-C

147509739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: missense_variant, undefined
orthologous variants: 43571153-G-T

147509772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: synonymous_variant, undefined
orthologous variants: 43571186-G-T

147509811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: synonymous variant
orthologous variants: 43571225-C-T

147509920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 43571332-G-A

147509920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 43571332-G-C

147509920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 43571332-G-T

147510013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3015
most severe consequence: 5 prime UTR variant
orthologous variants: 43571424-C-T