7717822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 5 prime UTR variant
orthologous variants: 69437283-G-A

7717822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 5 prime UTR variant
orthologous variants: 69437283-G-C

7717822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 5 prime UTR variant
orthologous variants: 69437283-G-T

7717838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 69437267-G-A

7717838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 69437267-G-T

7717909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69437207-G-A

7717971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69437153-G-A

7717971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69437153-G-T

7717972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69437152-G-A

7717972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69437152-G-T

7717974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69437150-G-A

7717974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69437150-G-T

http://identifiers.org/hco/17/GRCh38#7717975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69437149-A-C

7717975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69437149-A-G

7717990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69437134-T-G

7717992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69437132-T-C

7718371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69436827-A-G

http://identifiers.org/hco/17/GRCh38#7718540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69436657-C-A

7718810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69436420-C-T

7718877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69436359-T-C

7718880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69436356-G-C

7718882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69436354-A-G

7718958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69436275-C-T

7719700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69435401-T-C

7719719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: splice acceptor variant
orthologous variants: 69435382-A-G

7719747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69435354-G-A

7719905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69435196-G-A

7719905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69435196-G-T

7719917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69435184-G-A

7719917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69435184-G-C

7719917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69435184-G-T

7719948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69435153-A-G

7721093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69433119-C-T

7721110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69433099-G-C

7721561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69428754-G-T

7721746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69428594-C-T

7721876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69428488-G-A

7721935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69428437-A-G

7726836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69420626-A-T

http://identifiers.org/hco/17/GRCh38#7726991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69420490-C-A

7726991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69420490-C-G

7726991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69420490-C-T

7726994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69420487-T-C

http://identifiers.org/hco/17/GRCh38#7727031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69420464-A-C

7727031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69420464-A-G

7727031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69420464-A-T

7727053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69420442-A-G

7727054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69420441-T-C

7727218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69420281-C-T

7727254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69420245-T-C

7727275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: synonymous variant
orthologous variants: 69420224-C-T

7727338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69420148-C-T

7727744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69419689-G-A

7727744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69419689-G-T

7727769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69419664-A-G

7732775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69415481-A-G

7732909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69415360-A-G

7733048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69415263-G-C

7733048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69415263-G-T

7733201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69415112-C-G

7733282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69415031-T-C

7733873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69412717-G-A

7733873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69412717-G-T

7733878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69412712-A-T

7733921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69412690-T-C

7733994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69412630-C-T

http://identifiers.org/hco/17/GRCh38#7734015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69412609-C-A

7734015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69412609-C-T

7734016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69412608-C-G

7734035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69412584-T-A

7734035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69412584-T-G

7734040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69412579-A-G

7734105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69412092-G-A

7734105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69412092-G-T

http://identifiers.org/hco/17/GRCh38#7734113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69412084-A-C

7734113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69412084-A-G

http://identifiers.org/hco/17/GRCh38#7734114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69412083-C-A

7734114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69412083-C-T

http://identifiers.org/hco/17/GRCh38#7734177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69412030-C-A

7734177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 69412030-C-T

7734352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69411856-G-C

7734352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69411856-G-T

7734520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69411724-G-C

7734637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69411607-G-A

http://identifiers.org/hco/17/GRCh38#7734746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69411500-A-C

7734746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69411500-A-T

7734750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69411496-G-A

http://identifiers.org/hco/17/GRCh38#7734823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69411433-C-A

7734823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69411433-C-G

7734823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69411433-C-T

7734860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69411408-T-A

7734860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69411408-T-C

7734860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69411408-T-G

7734938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69411316-G-A

7736210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69411177-A-G

7736448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69410957-C-T

7736452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69410953-T-C

7736532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69410882-G-T

7737306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69409067-G-A

7737306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69409067-G-T

7737311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69409062-T-C

7737440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69409009-G-A

7737475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69408978-G-T

7737509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69408943-A-G

http://identifiers.org/hco/17/GRCh38#7737936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69408576-C-A

7737936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69408576-C-T

http://identifiers.org/hco/17/GRCh38#7738865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69408000-C-A

7739062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69407786-C-T

7739651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69407579-G-T

7739718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69407518-T-C

7739922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69407315-C-G

http://identifiers.org/hco/17/GRCh38#7739955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69407284-C-A

7739955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69407284-C-G

7739955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69407284-C-T

7739983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69407257-G-A

7740034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69407208-T-A

7740034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69407208-T-C

7740034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69407208-T-G

http://identifiers.org/hco/17/GRCh38#7740066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69407172-C-A

7740066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69407172-C-G

7740066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69407172-C-T

http://identifiers.org/hco/17/GRCh38#7740078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69407160-C-A

7740078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69407160-C-G

7740078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69407160-C-T

7740122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69407114-T-G

7740247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69407070-C-T

7740295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69407031-G-A

7740295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69407031-G-T

7740347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69407002-G-A

7740347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69407002-G-T

7740358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69406999-A-G

7740430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69406925-G-A

7740430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: stop gained
orthologous variants: 69406925-G-T

7740560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69406795-C-T

7740587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69406782-G-A

7740587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69406782-G-T

7740590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69406779-T-C

7740590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69406779-T-G

http://identifiers.org/hco/17/GRCh38#7740734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69406692-C-A

7740734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69406692-C-T

7741061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69406377-G-T

http://identifiers.org/hco/17/GRCh38#7742920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69405725-C-A

7742920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 69405725-C-G

7742920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 69405725-C-T

7743084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69405558-A-G

http://identifiers.org/hco/17/GRCh38#7743237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69405399-C-A

http://identifiers.org/hco/17/GRCh38#7743241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69405395-C-A

7743241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, missense_variant
orthologous variants: 69405395-C-G

7743241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, missense_variant
orthologous variants: 69405395-C-T

7743260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 69405370-T-C

7743281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 69405270-T-C

http://identifiers.org/hco/17/GRCh38#7743292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69405259-C-A

7743292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, missense_variant
orthologous variants: 69405259-C-T

http://identifiers.org/hco/17/GRCh38#7743808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69404809-C-A

http://identifiers.org/hco/17/GRCh38#7743986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69404645-C-A

http://identifiers.org/hco/17/GRCh38#7743989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69404642-C-A

7743989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69404642-C-T

7744370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69404278-A-G

7744525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69404141-A-G

7744791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69403425-G-A

7744791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69403425-G-C

7747736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69402322-T-C

7747792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69402265-G-A

7748060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69402020-C-T

7748859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69401568-G-T

7749385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69401362-G-A

7749487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69401261-C-T

7749502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69401246-A-G

http://identifiers.org/hco/17/GRCh38#7749589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69401164-A-C

7750206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69400659-A-G

7750382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69400502-T-A

7750447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69399805-T-C

7750455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69399797-C-T

7750664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, undefined
orthologous variants: 69399593-C-T

http://identifiers.org/hco/17/GRCh38#7750804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#69399271-A-C

7751614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69398224-T-C

7751872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69397968-T-G

7753293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69395661-C-T

http://identifiers.org/hco/17/GRCh38#7753470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69395541-A-C

7753859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69395219-A-G

7753859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69395219-A-T

7753863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69395215-A-G

7754201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69394969-G-A

7754201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69394969-G-T

7754243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69394920-G-A

7754243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69394920-G-T

7754251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69394912-T-C

7754314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69394841-G-A

7754314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69394841-G-T

7757069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69391703-G-A

7757155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69391618-T-C

7757155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69391618-T-G

7757218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69391555-G-A

7757218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69391555-G-C

7757218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69391555-G-T

http://identifiers.org/hco/17/GRCh38#7757251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69391519-C-A

7757389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69391421-G-A

7757389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69391421-G-T

7757876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69391053-C-G

7757895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69391035-G-A

7757943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69390986-C-T

7758252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69390542-G-A

7758252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69390542-G-T

7758571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69390009-C-G

7758571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69390009-C-T

http://identifiers.org/hco/17/GRCh38#7758706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69389878-C-A

http://identifiers.org/hco/17/GRCh38#7758707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69389877-C-A

7758727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69389857-G-A

7758737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69389847-G-T

7758785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69389687-G-T

7758968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: synonymous variant
orthologous variants: 69389492-A-G

7759023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69389437-G-C

7759113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69389347-G-A

http://identifiers.org/hco/17/GRCh38#7759170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69389285-C-A

7759230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69389251-G-T

7759379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69388867-T-A

7759403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69388843-C-T

7759455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: synonymous variant
orthologous variants: 69388793-C-T

http://identifiers.org/hco/17/GRCh38#7759488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69388760-A-C

7759527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69388721-A-T

7759629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69388620-C-T

7759772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69387510-T-G

7759966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69387311-G-A

7759966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69387311-G-C

7759966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69387311-G-T

7760022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69387273-T-C

7760403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69387206-C-T

7760435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69387174-C-T

7760665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69386168-G-A

7760665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69386168-G-T

7760677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69386156-G-A

7760677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69386156-G-T

http://identifiers.org/hco/17/GRCh38#7760680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69386153-C-A

7760716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69386112-A-G

http://identifiers.org/hco/17/GRCh38#7761020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69385823-A-C

7763706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69384239-G-A

7763706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69384239-G-T

7763730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69384220-C-T

7763800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69384157-A-G

7763820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69384139-G-A

7763825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 69384135-T-C

7763994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 69383966-C-T

http://identifiers.org/hco/17/GRCh38#7764052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69383907-C-A

7764123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 69383630-C-T

7764265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 69383488-G-A

7764265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 69383488-G-C

7764334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69383423-G-T

7764414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69383353-G-T

7765369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69383138-C-G

7765656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69382859-G-A

7766159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69382670-T-C

7766199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69382648-T-C

7766223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69382624-G-T

7766283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69382556-G-A

7766326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 69382482-A-T

http://identifiers.org/hco/17/GRCh38#7766332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69382476-A-C

http://identifiers.org/hco/17/GRCh38#7766344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69382464-A-C

7766344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 69382464-A-G

7766374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 69382434-C-T

7766454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 69382354-C-T

7766492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69382316-G-A

7766492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69382316-G-T

http://identifiers.org/hco/17/GRCh38#7766493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69382315-A-C

7766523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69382286-G-A

7766523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69382286-G-T

7766590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69382239-G-A

7766590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69382239-G-T

7766592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69382237-G-C

7766592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69382237-G-T

7766600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69382229-T-A

7766808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69382050-T-C

7767222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69378809-G-A

http://identifiers.org/hco/17/GRCh38#7767599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69378463-A-C

7767599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69378463-A-T

7767753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69378311-G-T

7767786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69378286-C-T

http://identifiers.org/hco/17/GRCh38#7767833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69378263-C-A

7767833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69378263-C-G

7767833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69378263-C-T

7767879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69378199-A-G

7768130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69377920-G-A

7768130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69377920-G-C

7768135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69377915-G-A

7768135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69377915-G-T

http://identifiers.org/hco/17/GRCh38#7768301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69377751-C-A

7768301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69377751-C-G

7770196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69375345-A-G

http://identifiers.org/hco/17/GRCh38#7770229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69375285-C-A

7770229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69375285-C-T

7770435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69375000-A-T

7770472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69374976-T-C

7770531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69374916-C-T

7770617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69374830-G-A

7770686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69374770-G-A

7771238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69374292-T-C

7771286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69374244-G-A

7771294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69374236-G-A

http://identifiers.org/hco/17/GRCh38#7771302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69374228-C-A

7771313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69374217-A-G

http://identifiers.org/hco/17/GRCh38#7771314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69374216-C-A

7771314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69374216-C-T

7771369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69374161-A-G

7772441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69373521-A-G

7772443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69373519-G-T

7772495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69373469-C-T

7772582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69373373-C-G

http://identifiers.org/hco/17/GRCh38#7774640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69370563-C-A

7775008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69370237-G-A

7775021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69370224-G-A

7775021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69370224-G-T

7775055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69370176-T-G

7775109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69370126-T-C

7775129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69370106-A-T

7775197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69369688-A-G

7775199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69369686-G-A

7775199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69369686-G-C

7775199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69369686-G-T

7775316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69369573-T-C

7775348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69369541-T-C

http://identifiers.org/hco/17/GRCh38#7775683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69369449-C-A

7775708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69369422-A-G

http://identifiers.org/hco/17/GRCh38#7775941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69369080-C-A

7775941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69369080-C-T

7775942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69369079-T-C

7775962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69369036-T-C

7775969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69369029-G-T

7776640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69368694-G-T

http://identifiers.org/hco/17/GRCh38#7776689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69368652-C-A

7776740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69368618-A-G

http://identifiers.org/hco/17/GRCh38#7776857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69368501-A-C

http://identifiers.org/hco/17/GRCh38#7776898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69368460-C-A

7776898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69368460-C-T

http://identifiers.org/hco/17/GRCh38#7776987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69368453-C-A

7776987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69368453-C-G

7777175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69368433-T-G

7777179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69368429-T-G

7777299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69368348-G-A

7777299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69368348-G-T

7777372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69368244-G-A

7777372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69368244-G-T

7777646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69367970-G-A

7777646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69367970-G-C

http://identifiers.org/hco/17/GRCh38#7777679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69367936-C-A

7777718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69367908-G-C

http://identifiers.org/hco/17/GRCh38#7777753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69367873-C-A

7777753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69367873-C-T

http://identifiers.org/hco/17/GRCh38#7777989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69367635-C-A

7777989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69367635-C-T

7778008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69367616-C-T

http://identifiers.org/hco/17/GRCh38#7778064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69367555-C-A

7778576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69367043-G-A

7778576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69367043-G-T

7778620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69366990-G-T

http://identifiers.org/hco/17/GRCh38#7778814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69366873-C-A

7778862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69366842-C-T

7779170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69366549-G-A

7779170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69366549-G-T

7779172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69366547-G-T

7779196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69366524-T-C

7779339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69366374-G-A

7779438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69366275-G-A

7779438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69366275-G-C

7779447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69366266-A-G

7779470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69366240-G-A

7779470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69366240-G-C

http://identifiers.org/hco/17/GRCh38#7779505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69366211-C-A

7779505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69366211-C-T

http://identifiers.org/hco/17/GRCh38#7779513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69366203-A-C

http://identifiers.org/hco/17/GRCh38#7779516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69366200-C-A

7779516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69366200-C-G

7779516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69366200-C-T

7779725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69365551-A-G

7779875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69365397-A-G

7780047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69365243-T-C

7780047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69365243-T-G

7780128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69365179-G-T

7780341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69364984-T-C

7780352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69364973-G-A

7780407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69364919-G-C

7780407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69364919-G-T

7780423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69364903-G-T

http://identifiers.org/hco/17/GRCh38#7780480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69364833-C-A

7780480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69364833-C-G

http://identifiers.org/hco/17/GRCh38#7780524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69364792-C-A

7780524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69364792-C-T

http://identifiers.org/hco/17/GRCh38#7780555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69364760-C-A

7780555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69364760-C-T

7780583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69364740-G-A

7780583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69364740-G-C

7780583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69364740-G-T

7780652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69364674-C-G

7780652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69364674-C-T

7780717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69364609-C-G

7780792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69364534-G-A

7780878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69364443-G-T

7780885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69364436-T-C

http://identifiers.org/hco/17/GRCh38#7780908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69364411-C-A

7780908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69364411-C-T

7780913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69364406-G-C

http://identifiers.org/hco/17/GRCh38#7780968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69364358-C-A

7780968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69364358-C-T

7781533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69363721-T-C

http://identifiers.org/hco/17/GRCh38#7781599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69363657-C-A

7781927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69363225-G-A

7782277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 69362895-C-T

7782366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 69362812-A-G

7782466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 69362718-G-A

http://identifiers.org/hco/17/GRCh38#7785978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69356749-A-C

7785978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69356749-A-G

7786152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69356595-G-A

7786205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69356542-T-C

7786418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69356365-A-G

http://identifiers.org/hco/17/GRCh38#7786447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69356355-C-A

7786447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69356355-C-T

7786457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69356345-G-A

7786457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69356345-G-C

7786457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69356345-G-T

7786618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69356165-G-A

7786630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69356153-A-G

7786630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69356153-A-T

7786695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 69356088-G-C

http://identifiers.org/hco/17/GRCh38#7786701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69356082-C-A

7786701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69356082-C-T

7786722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69356063-G-A

7786836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69355942-G-A

7786877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 69355905-A-G

7786908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69355869-G-A

7786908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69355869-G-C

7786935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69355842-C-G

7786935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69355842-C-T

7786998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 69355779-C-T

7787049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69355735-G-A

7787102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69355683-G-A

7787102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69355683-G-T

http://identifiers.org/hco/17/GRCh38#7787111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69355671-C-A

7787212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69355485-G-A

7787212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69355485-G-T

7787259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69355428-G-A

7787259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69355428-G-T

http://identifiers.org/hco/17/GRCh38#7787275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69355412-C-A

7787275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69355412-C-T

7787278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69355409-T-C

7787278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69355409-T-G

7787288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69355401-G-A

7787288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69355401-G-T

7787316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69355373-T-A

7787316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69355373-T-C

7787321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69355367-T-C

http://identifiers.org/hco/17/GRCh38#7787360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69355216-A-C

7787360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69355216-A-G

7787360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69355216-A-T

7787433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69355078-G-A

7787433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69355078-G-T

7787640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69354899-G-T

7787653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69354883-T-C

7787668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69354862-G-A

7787668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 69354862-G-T

http://identifiers.org/hco/17/GRCh38#7788071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69354313-C-A

7788086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 69354298-G-C

7788172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: synonymous variant
orthologous variants: 69354212-G-A

7788179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69354205-C-T

7788227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69354157-G-C

http://identifiers.org/hco/17/GRCh38#7788287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69354090-C-A

7788287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69354090-C-T

http://identifiers.org/hco/17/GRCh38#7788386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69354027-C-A

7788406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69353927-G-C

7788408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69353925-G-T

7788410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69353923-G-A

7788410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69353923-G-T

7789062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69353255-G-T

7789080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69353232-C-T

7789083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69353229-G-T

7789163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69353172-C-T

7789176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69353159-A-G

7789184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69353151-C-T

7791872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69350209-G-A

http://identifiers.org/hco/17/GRCh38#7792171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69349863-C-A

7792171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69349863-C-T

http://identifiers.org/hco/17/GRCh38#7792172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69349862-C-A

7792172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69349862-C-T

7792187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69349847-C-G

7792235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69349800-C-T

7792297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69349736-A-T

7792330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69349703-C-T

7792362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69349670-T-A

7792362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69349670-T-C

7792411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69349642-T-C

http://identifiers.org/hco/17/GRCh38#7792530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69349529-C-A

7792530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69349529-C-T

7792835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69349204-G-A

7792835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69349204-G-C

7792847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69349192-T-C

7792857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: splice donor variant
orthologous variants: 69349182-T-C

7792861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69349178-T-C

7792917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69349103-C-T

7792918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69349102-C-T

7792940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69349094-T-C

7792957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69349058-A-G

7792957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69349058-A-T

http://identifiers.org/hco/17/GRCh38#7793029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69348986-C-A

7793029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: stop gained
orthologous variants: 69348986-C-T

http://identifiers.org/hco/17/GRCh38#7793032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69348983-A-C

7793170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69348845-T-G

7793177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69348838-G-A

7793214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348801-C-G

7793214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348801-C-T

7793251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348792-G-T

7793252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348791-A-T

7793254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348789-A-G

7793272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348768-A-G

7793275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348765-G-A

7793275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348765-G-T

7793277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348763-G-A

7793303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348735-T-C

http://identifiers.org/hco/17/GRCh38#7793310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69348728-C-A

7793310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348728-C-T

7793338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348666-G-A

7793338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348666-G-T

7793345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348660-G-A

7794246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 69348277-C-T

7794363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348160-G-A

7794363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348160-G-C

http://identifiers.org/hco/17/GRCh38#7794417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69348112-C-A

7794417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348112-C-T

7794447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348071-G-A

7794447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348071-G-C

7794447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348071-G-T

7794486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348035-G-A

7794509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348013-G-A

7794509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69348013-G-T

7794606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69347912-C-T

7794774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69347750-A-G

7794774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69347750-A-T

7796587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, missense_variant
orthologous variants: 69346680-G-A

7796587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, missense_variant
orthologous variants: 69346680-G-C

7796587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, missense_variant
orthologous variants: 69346680-G-T

7796660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 69346607-G-A

7796888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69345460-A-G

7796922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69345426-T-A

http://identifiers.org/hco/17/GRCh38#7797042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69345335-C-A

7797042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69345335-C-T

7797068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69345308-G-A

7797068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69345308-G-C

7797068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69345308-G-T

http://identifiers.org/hco/17/GRCh38#7797133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69345282-A-C

7797133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69345282-A-G

7797133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69345282-A-T

http://identifiers.org/hco/17/GRCh38#7797134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69345281-A-C

http://identifiers.org/hco/17/GRCh38#7797700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69344729-A-C

7797700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69344729-A-G

7797715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69344714-C-T

7797838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69344591-C-T

http://identifiers.org/hco/17/GRCh38#7797951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69344500-C-A

7797951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69344500-C-G

7797951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69344500-C-T

7797969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69344438-G-A

7797969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69344438-G-C

7797969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69344438-G-T

7798025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69344281-G-A

7798097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69344207-C-G

7798097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69344207-C-T

7798199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69344110-T-C

7798204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: synonymous variant
orthologous variants: 69344105-C-T

7798321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69343988-G-C

7798321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69343988-G-T

7798507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69343858-C-T

7798738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69343625-C-T

7798779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69343587-A-G

7798851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69343528-T-A

7799052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69343421-G-T

7799112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69343361-C-T

7799258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69343223-T-A

7799258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69343223-T-G

7799272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69343207-C-T

7799286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69343193-C-T

7801187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69342538-T-C

7801191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69342534-G-A

7801259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69342470-T-C

7801330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69342404-A-G

7801333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69342401-G-A

7801350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69342381-A-T

http://identifiers.org/hco/17/GRCh38#7801457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69342288-C-A

7801457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69342288-C-G

7801457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69342288-C-T

7801482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69342264-A-G

7801482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69342264-A-T

7801807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69341999-C-G

7801807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69341999-C-T

7801971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69341869-T-C

http://identifiers.org/hco/17/GRCh38#7802047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69341796-C-A

7802065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69341779-T-A

7802087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69341754-A-G

7802231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69341549-C-G

7803433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69340154-G-A

7803851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69339818-A-G

7803954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69339701-A-G

7804134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, undefined
orthologous variants: 69339547-G-A

7804134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, undefined
orthologous variants: 69339547-G-T

7804138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, undefined
orthologous variants: 69339543-T-A

7804164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69339518-G-T

http://identifiers.org/hco/17/GRCh38#7804166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69339516-C-A

7804166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69339516-C-G

7804166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69339516-C-T

7804188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69339494-G-A

7804317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69339365-T-C

7804359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: synonymous_variant, undefined
orthologous variants: 69339323-T-C

7804425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69339257-A-G

7804455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69339227-G-A

7804455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: stop gained
orthologous variants: 69339227-G-T

7804472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69339210-G-A

http://identifiers.org/hco/17/GRCh38#7804484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69339207-A-C

http://identifiers.org/hco/17/GRCh38#7804489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69339202-C-A

7804489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69339202-C-T

http://identifiers.org/hco/17/GRCh38#7804490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69339201-C-A

7804490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69339201-C-G

7804490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69339201-C-T

7804491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69339200-G-A

7804491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69339200-G-C

http://identifiers.org/hco/17/GRCh38#7804534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69339185-A-C

7804534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69339185-A-G

http://identifiers.org/hco/17/GRCh38#7804887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69339124-C-A

7804887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69339124-C-G

http://identifiers.org/hco/17/GRCh38#7804909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69339102-C-A

7804909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69339102-C-T

7804925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69339086-G-T

7804948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69339064-T-C

7804958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 69339054-G-A

7805042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, missense_variant
orthologous variants: 69338970-G-A

7805151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69338878-C-G

7805198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69338822-G-T

7805398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69338615-G-A

7805402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69338611-G-A

7805431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69338582-C-T

7806798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69337917-G-T

7806910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69337782-G-A

7807067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69337660-T-C

7807068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69337659-G-T

7807104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69337623-G-A

7807104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69337623-G-T

7807105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69337622-A-G

http://identifiers.org/hco/17/GRCh38#7807116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69337599-C-A

7807209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69337509-G-T

7807359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69337361-A-G

7807366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69337354-G-T

7807426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69337261-G-A

7807426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69337261-G-T

7807434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69337254-G-A

7807434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69337254-G-T

7807521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69337168-G-A

7807611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69337079-A-T

7807678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69337015-G-A

7807678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69337015-G-T

7807691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69337006-T-C

7807691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69337006-T-G

7807802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69336910-G-A

http://identifiers.org/hco/17/GRCh38#7808024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69336685-A-C

7809622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69334394-G-A

7812165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69330636-G-A

7816249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69329455-T-G

7816251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69329453-G-T

7816433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69329255-A-G

7816446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69328906-G-A

7816446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69328906-G-C

7816446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69328906-G-T

7816715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69328641-A-G

7816721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: stop gained
orthologous variants: 69328635-G-T

http://identifiers.org/hco/17/GRCh38#7816806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69328574-C-A

7816811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69328569-G-C

7816811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69328569-G-T

7816841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69328539-G-A

7816841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69328539-G-T

7817162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69328253-A-G

7817191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69328226-A-G

http://identifiers.org/hco/17/GRCh38#7817274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69328136-C-A

7817274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69328136-C-T

http://identifiers.org/hco/17/GRCh38#7817434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69327977-A-C

7817434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69327977-A-G

7817488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69327945-G-A

7817666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69327789-G-A

7817699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: stop gained
orthologous variants: 69327756-C-T

7817773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69327689-C-T

7817814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: synonymous variant
orthologous variants: 69327647-G-A

7817814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69327647-G-C

7817851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69327610-G-A

http://identifiers.org/hco/17/GRCh38#7817997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69327407-C-A

7817997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69327407-C-G

7817997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69327407-C-T

7818113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69327274-A-G

7818145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69327256-G-C

7818217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69327210-A-G

http://identifiers.org/hco/17/GRCh38#7818233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69327194-C-A

7818233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69327194-C-G

7818233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69327194-C-T

http://identifiers.org/hco/17/GRCh38#7818234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69327193-C-A

7818234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69327193-C-T

7818329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69327093-C-T

7818355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: stop gained
orthologous variants: 69327067-T-A

7818355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: synonymous variant
orthologous variants: 69327067-T-C

7818489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69326935-C-T

7818492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69326934-G-A

7818492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69326934-G-C

7818492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69326934-G-T

7818497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69326929-A-G

7818709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69326724-G-T

http://identifiers.org/hco/17/GRCh38#7818769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69326664-A-C

7818769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69326664-A-G

7818769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69326664-A-T

7818810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69326615-G-A

7818821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69326604-C-T

7818904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69326537-T-G

http://identifiers.org/hco/17/GRCh38#7818992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69326449-A-C

7819068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69326373-G-A

7819068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69326373-G-T

7819086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69326354-C-T

http://identifiers.org/hco/17/GRCh38#7819131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69326307-C-A

7819131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69326307-C-T

7819154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69326284-C-T

7819371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69326065-G-A

7820193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69324670-C-T

7821168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69323898-G-A

7821407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69323642-T-C

7821545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69323529-G-T

7823202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69322282-G-A

7823268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69322245-T-A

http://identifiers.org/hco/17/GRCh38#7823344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69322190-A-C

7823359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69322175-G-A

7823359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69322175-G-T

7823610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense_variant, undefined
orthologous variants: 69321901-G-A

7823676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, undefined
orthologous variants: 69321828-C-T

7823683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, undefined
orthologous variants: 69321822-A-G

7823683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron_variant, undefined
orthologous variants: 69321822-A-T

7823693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69321812-T-C

7823905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69321651-G-T

7824068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69321517-C-T

7824145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69321457-T-C

7824175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69321427-G-A

http://identifiers.org/hco/17/GRCh38#7824341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69320427-C-A

7824341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69320427-C-T

http://identifiers.org/hco/17/GRCh38#7824377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69320390-C-A

7824377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69320390-C-G

7824377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69320390-C-T

7824528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69320325-T-C

7824572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: synonymous variant
orthologous variants: 69320281-C-T

7824757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69320097-A-G

http://identifiers.org/hco/17/GRCh38#7824761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69320093-C-A

http://identifiers.org/hco/17/GRCh38#7824873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69319985-A-C

7829636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69315510-T-C

7829911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69315221-A-G

7830039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69315140-A-G

7830053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69315126-G-T

7830164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69315018-T-A

7830164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69315018-T-C

7830167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69315015-A-G

http://identifiers.org/hco/17/GRCh38#7830180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69314995-C-A

7830180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69314995-C-T

7830197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69314978-T-A

7830216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69314961-A-G

7830230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69314943-A-G

7830345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69314834-C-G

7830345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69314834-C-T

http://identifiers.org/hco/17/GRCh38#7830518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69314660-C-A

7830518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69314660-C-T

7830542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69314635-T-C

http://identifiers.org/hco/17/GRCh38#7830784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69314389-C-A

7830784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: synonymous variant
orthologous variants: 69314389-C-T

7830884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69314252-A-G

7830899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69314224-G-A

7830899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69314224-G-C

7830910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69314213-T-C

7830910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69314213-T-G

7831031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69314085-G-A

7831066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69314053-A-G

7831287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69313832-G-C

7831380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69313741-G-A

7831831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69313310-G-A

7831831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69313310-G-T

7831850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69313291-T-C

7832568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69312741-T-A

7832568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69312741-T-G

7832723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: missense variant
orthologous variants: 69312586-G-A

7833004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69312309-G-A

7833004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69312309-G-T

7833027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69312286-A-G

7833286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69312043-T-C

7833326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: intron variant
orthologous variants: 69312019-C-T

http://identifiers.org/hco/17/GRCh38#7833537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#69311813-C-A

7833537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3 prime UTR variant
orthologous variants: 69311813-C-G

7833710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2948
most severe consequence: 3 prime UTR variant
orthologous variants: 69311665-G-T