157259820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65962386-T-C

157259839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65962405-A-T

157259864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65962428-G-C

http://identifiers.org/hco/3/GRCh38#157259938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65962501-C-A

157259938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65962501-C-T

157260193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65962718-A-G

157260391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65962931-G-T

157260428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65962969-T-C

157260845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65964268-A-T

http://identifiers.org/hco/3/GRCh38#157260856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65964278-C-A

157260856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65964278-C-T

http://identifiers.org/hco/3/GRCh38#157260870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65964291-A-C

157260870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65964291-A-G

157260870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65964291-A-T

http://identifiers.org/hco/3/GRCh38#157260872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65964293-C-A

http://identifiers.org/hco/3/GRCh38#157260891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65964311-C-A

157260918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65964326-G-A

157260918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65964326-G-T

157260931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65964341-T-C

157260931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65964341-T-G

157260955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65964365-T-C

http://identifiers.org/hco/3/GRCh38#157260993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65964403-C-A

157260993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65964403-C-G

157261041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65964447-A-G

157261097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65964489-C-T

157261127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65964519-T-A

157261127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65964519-T-C

157261257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 65964649-G-T

157261352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 65964744-A-T

157261448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65964837-A-G

http://identifiers.org/hco/3/GRCh38#157261459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65964847-A-C

http://identifiers.org/hco/3/GRCh38#157261469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65964857-C-A

157261489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65964877-T-A

157261489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65964877-T-G

157261495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65964882-T-C

157261518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65964906-T-A

157261576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65964961-C-T

157261658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65965058-A-G

157261658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65965058-A-T

157261680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65965080-C-T

157261814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65965185-T-C

157261907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65965263-C-G

157261939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65965293-A-G

http://identifiers.org/hco/3/GRCh38#157262031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65965369-A-C

157262051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65965388-T-C

157262094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65965430-C-T

http://identifiers.org/hco/3/GRCh38#157262197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65965527-C-A

157262462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65966081-C-T

157262586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65966392-G-A

157262586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65966392-G-C

157262840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65966676-C-G

157262938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65966778-C-T

157263010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65966850-C-G

157263477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65967217-A-G

157263951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65967697-A-T

http://identifiers.org/hco/3/GRCh38#157265575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65968526-C-A

157265575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 65968526-C-T

157265696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65968646-T-C

http://identifiers.org/hco/3/GRCh38#157265764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65968714-C-A

157265796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65968946-T-G

157265867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65969013-C-T

157266440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65970071-A-T

157266466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65970095-G-T

157266645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65970281-T-C

157266718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65970348-T-C

http://identifiers.org/hco/3/GRCh38#157266839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65970470-A-C

157266882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65970513-C-G

157267429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65970674-T-C

157267465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65970725-G-C

157267926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65970879-G-A

http://identifiers.org/hco/3/GRCh38#157267947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65970896-C-A

157268014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65970962-C-T

157269236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65971418-C-T

157269305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65971495-A-G

157269491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65971672-G-C

157269605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65971781-A-T

157269621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65971787-T-G

157269698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65971834-C-T

157269753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65971875-G-A

http://identifiers.org/hco/3/GRCh38#157270555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65972259-A-C

157270614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65972317-G-C

157270614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65972317-G-T

157270855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65972540-C-T

157270876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65972560-T-A

157270876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65972560-T-G

157271342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65972942-T-C

157274690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65973164-G-A

157274692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65973166-G-A

157274743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65973237-T-A

157274941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65973354-T-C

157275093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65973477-C-G

http://identifiers.org/hco/3/GRCh38#157275095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65973479-C-A

157275095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65973479-C-G

157275097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65973481-G-A

157275195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65973753-T-G

157275865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65974003-G-T

157276157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65974257-A-G

157276403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65974501-T-G

157277618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65977232-A-T

157277769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65977419-C-T

157277792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65977463-T-C

157280886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65987502-C-G

157280929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65987523-A-G

157281062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65987666-A-G

157281078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65987682-A-G

157281080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65987684-A-G

157281080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65987684-A-T

157281082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65987686-G-A

157281096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65987700-G-A

157281104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65987708-G-A

157281104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65987708-G-C

157282483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65988575-T-C

157282533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65988625-A-G

157282611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 65988736-C-T

157282624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 65988749-T-C

157282631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 65988756-C-T

157282648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65988779-T-A

157282750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65988888-A-G

157282851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65988988-C-T

157283221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 65989336-C-T

157283599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65989401-T-C

http://identifiers.org/hco/3/GRCh38#157283672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65989474-C-A

157283672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65989474-C-T

157284050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65990239-C-G

157284050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65990239-C-T

157284052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65990241-C-T

157284607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65990797-A-G

157284977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 65991146-G-T

http://identifiers.org/hco/3/GRCh38#157284980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65991149-C-A

157284980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 65991149-C-G

157285095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65991264-T-A

http://identifiers.org/hco/3/GRCh38#157285123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65991295-C-A

157285177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65991351-T-C

157285242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65991416-T-C

157285306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65991480-G-T

157285379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65991553-A-G

http://identifiers.org/hco/3/GRCh38#157286044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65994443-C-A

157286072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65994471-G-A

157286072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65994471-G-T

157286162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65994534-G-A

157286249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65994627-C-G

157286282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65994658-A-G

http://identifiers.org/hco/3/GRCh38#157286434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65994990-C-A

157286458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65995017-A-T

http://identifiers.org/hco/3/GRCh38#157286467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65995025-C-A

157286467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65995025-C-T

http://identifiers.org/hco/3/GRCh38#157286479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65995037-C-A

157286512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65995079-A-G

157286528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65995095-G-A

157286528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65995095-G-T

157286710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65995275-T-C

http://identifiers.org/hco/3/GRCh38#157286805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65995354-C-A

157286805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65995354-C-T

157286859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65995410-C-G

157286859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65995410-C-T

157286865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65995419-G-T

157286917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65995464-G-C

http://identifiers.org/hco/3/GRCh38#157287966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65995798-C-A

157288255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65996057-G-A

157288258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65996060-C-G

157288258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65996060-C-T

157288423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65996223-C-T

157288834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65997130-G-C

157288834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65997130-G-T

157288864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65997160-G-A

157288864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65997160-G-C

157288878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65997174-C-T

157288969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65997314-A-G

157289162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65997512-A-G

157289198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65997547-T-C

157289266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65997610-G-T

157289351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65997699-G-A

157289568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65997924-C-G

157289739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65998093-C-G

157289950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65998295-T-C

157289950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65998295-T-G

157289979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65998318-C-T

157290033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65998363-C-T

157290422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65998552-G-A

157290561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65998641-G-A

157291064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65999354-T-C

157291417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65999692-G-C

157291433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65999709-T-C

157291534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65999815-T-C

157291688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65999941-T-G

http://identifiers.org/hco/3/GRCh38#157291943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66000283-C-A

157292009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66000468-T-G

157292111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66000561-G-A

157292111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66000561-G-T

http://identifiers.org/hco/3/GRCh38#157292253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66000657-C-A

157292253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66000657-C-T

157292269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66000673-G-A

157292269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66000673-G-T

157292392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66000794-A-G

157293229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66001009-G-A

http://identifiers.org/hco/3/GRCh38#157293231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66001011-A-C

157293355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66001125-G-A

157293530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66001275-T-G

157293545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66001290-G-A

157294912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66005964-G-A

157294995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66006051-C-G

157295539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66007502-A-T

157296242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66008052-G-A

http://identifiers.org/hco/3/GRCh38#157296715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66008864-A-C

157297195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66009176-A-G

157297215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66009196-T-C

157297537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66009512-G-A

157297745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66009718-T-C

157297971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66009943-C-T

157298145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66010170-C-T

157298183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66010208-C-G

157298183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66010208-C-T

157298304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66010322-G-A

157298978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66011643-T-C

157299028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66011694-T-G

157299040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66011706-C-G

157299040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66011706-C-T

157300396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66013117-C-T

157300439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66013156-G-A

157300439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66013156-G-C

157300471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66013187-G-A

157300542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66013256-T-C

157300542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66013256-T-G

157300636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66013348-G-A

http://identifiers.org/hco/3/GRCh38#157300748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66013466-C-A

157300819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66013535-A-G

157300881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66013594-G-T

157303709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66014970-A-G

157304708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66016132-G-T

157304718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66016122-A-G

157310547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66024321-G-T

157310587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66024360-A-G

157310693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66024466-C-G

157310693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66024466-C-T

157310713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66024486-C-G

157311023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66024748-T-A

157311088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66024794-T-A

157311171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66024927-T-C

157311334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66025076-C-T

http://identifiers.org/hco/3/GRCh38#157311376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66025144-A-C

157311526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66025315-T-C

157311564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66025345-A-G

157311794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66025566-T-G

157313471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66028863-T-C

http://identifiers.org/hco/3/GRCh38#157313675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66029062-C-A

157313675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 66029062-C-G

http://identifiers.org/hco/3/GRCh38#157313783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66029169-A-C

http://identifiers.org/hco/3/GRCh38#157314552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66029564-A-C

157315088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66030067-A-G

157315513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66030460-A-G

http://identifiers.org/hco/3/GRCh38#157315721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66030663-C-A

157316399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66032617-G-T

157316548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66032765-G-A

157316548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66032765-G-C

157316648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66032865-A-G

157316683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66032899-A-G

157316789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66033002-T-G

http://identifiers.org/hco/3/GRCh38#157316992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66033180-A-C

157317039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66033227-T-C

157317117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66033305-A-G

157317204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 66033392-A-G

157317350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66033542-G-T

157319890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66033862-T-C

157331503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66034331-A-G

http://identifiers.org/hco/3/GRCh38#157331665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66034494-C-A

157331733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66034580-A-G

157331810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66034615-G-A

157331832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66034636-T-C

157331874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66034678-C-T

157332006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66034761-C-G

157332804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66038430-T-G

157335444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66042943-A-G

157335444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66042943-A-T

157335738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66043213-C-T

157335786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66043270-G-A

157335786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66043270-G-T

157335835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66043320-A-G

157335837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66043322-C-T

157335926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66043360-C-G

157335926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66043360-C-T

157336071-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66043477-A-T

157336251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66043642-T-C

157337613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66044107-C-T

157337656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66044148-G-A

157339780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66044947-T-C

157339985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66045125-G-C

157346411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66045387-C-T

157346419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66045395-A-G

157346499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66045473-A-T

157347224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66045876-T-A

157352383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66047214-T-C

157352605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66053743-G-C

157352631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66053769-T-C

157352897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66054015-G-C

157352958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66054225-G-C

157353039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66054324-A-G

157353041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66054326-C-T

157353118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66054403-G-A

157353118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66054403-G-C

http://identifiers.org/hco/3/GRCh38#157353233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66054629-C-A

157353238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66054634-G-A

157353618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66054701-C-G

157353620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66054703-A-T

157353626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66054709-T-C

157353627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66054710-T-C

157353688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66054759-G-A

157353688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66054759-G-T

157353727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66054799-C-G

157353730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66054802-A-G

157353732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66054804-C-T

157353748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66054820-A-G

157353784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66055260-A-G

157353962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66055426-G-T

157355553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66059177-C-T

157355560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66059185-G-T

http://identifiers.org/hco/3/GRCh38#157355730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66059323-C-A

157356561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66060279-T-A

157356598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66060317-T-A

157356929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66060582-A-G

157356935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66060588-T-C

157357017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66060665-T-A

157357103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66060729-C-T

157357132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66060757-G-C

157357132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66060757-G-T

157357184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66060808-A-G

157357197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66060821-C-T

157357421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66061046-C-T

157357944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66061220-T-C

157358043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66061328-G-A

157358044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66061329-T-A

157358055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66061340-G-C

157358074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66061359-T-C

157358158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66061427-A-G

157358518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66062002-A-T

157358631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66062547-G-A

157358645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66062562-A-T

157359815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66063383-A-G

157359838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66063408-A-T

157359912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66063477-C-G

157360008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66063577-T-A

157360008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66063577-T-C

157360478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66064028-T-C

http://identifiers.org/hco/3/GRCh38#157361072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66064327-C-A

157361353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66064560-T-A

157361594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66064731-G-A

157361594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66064731-G-C

157361814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66064904-A-G

157361976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66065060-C-T

157362379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66065136-T-C

157363419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 66065386-T-C

157363458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 66065425-G-A

157363478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66065445-T-C

http://identifiers.org/hco/3/GRCh38#157363552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66065519-A-C

157363552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66065519-A-G

157363600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66065567-C-T

157363689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 66065656-C-T

157363698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 66065665-A-G

157363721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66065688-C-T

157364157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66066500-G-T

157364185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66066528-G-T

157364226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66066572-C-T

http://identifiers.org/hco/3/GRCh38#157364288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66066633-C-A

157364454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66066801-C-T

157364520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 66066868-A-G

157364520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 66066868-A-T

157364531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66066879-T-C

157364531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66066879-T-G

157364547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66066895-T-A

http://identifiers.org/hco/3/GRCh38#157364558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66066906-C-A

http://identifiers.org/hco/3/GRCh38#157364654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66067004-C-A

157364654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66067004-C-G

157364654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66067004-C-T

157364685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66067037-C-T

157365302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66068491-C-T

157365518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66068685-C-T

http://identifiers.org/hco/3/GRCh38#157365597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66068763-C-A

157365626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66068800-T-G

157369294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66069485-C-T

157369389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66069629-G-A

157369559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66069813-G-A

157369877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66070081-G-A

157370138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66070326-T-C

157370224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66070411-C-G

157370310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66070497-G-C

157370334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66070521-A-G

157371455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66071079-G-T

157371488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66071111-G-A

157371488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66071111-G-T

157371502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66071125-C-T

http://identifiers.org/hco/3/GRCh38#157371745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66071342-C-A

157371745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66071342-C-G

157371785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66071385-T-C

157371931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66071559-T-C

157372102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66071697-A-T

157372567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66072431-T-C

157373035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66072786-G-T

157373217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66073700-C-T

157373249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66073734-A-G

157373661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66074086-C-T

157373700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66074113-G-A

157373787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66074198-T-C

157373832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66074232-C-T

157373834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66074234-T-G

157373849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66074249-A-G

157373864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66074264-T-C

http://identifiers.org/hco/3/GRCh38#157373932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66074331-A-C

http://identifiers.org/hco/3/GRCh38#157374117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66074515-C-A

157374177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66074570-A-G

157374289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66074669-T-C

157374333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66074717-G-A

157374362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66074745-A-T

157374674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66075051-A-G

157376349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66076831-A-G

157376441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66076927-T-C

157376701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66077178-G-T

157377062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66077540-T-C

157377249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66077715-C-T

157380175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66078437-G-A

http://identifiers.org/hco/3/GRCh38#157380288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66078547-C-A

157380414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66078666-A-G

157380419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66078670-C-T

157380537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66078796-G-T

157380587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66078846-C-T

157380773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66079033-T-C

157381005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66079219-A-T

157381022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66079236-A-T

157381060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66079274-T-C

157381063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66079277-G-A

157381063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66079277-G-T

157381190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 66079421-G-A

157381190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 66079421-G-T

157381236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 66079467-G-A

157381236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66079467-G-C

157381350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, synonymous_variant
orthologous variants: 66079581-G-A

157381350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, stop_gained
orthologous variants: 66079581-G-C

157381354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66079585-G-A

157381354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66079585-G-T

157381365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66079596-C-G

157384350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66080133-G-A

157384427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66080228-T-G

157384813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66080706-G-A

157385210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66081083-T-A

157385210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66081083-T-C

157385297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66081150-G-A

http://identifiers.org/hco/3/GRCh38#157385365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66081215-C-A

157385407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66081257-G-A

157386129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66089899-G-A

157386280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66090034-T-A

157386280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66090034-T-G

157386541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66090282-G-C

157386793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66090527-T-A

157387007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66090740-C-T

157387135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66090864-G-C

157387237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66090961-G-A

157387304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66091024-G-T

157387417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66091129-G-A

157387449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66091140-C-T

157389193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66097024-A-G

157389193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66097024-A-T

157389204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66097035-G-T

157389700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66097673-C-T

http://identifiers.org/hco/3/GRCh38#157389839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66097812-C-A

157389839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66097812-C-T

157389910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66097966-T-C

157390117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66098112-G-C

157399954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66100754-T-G

157400104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66100898-T-C

http://identifiers.org/hco/3/GRCh38#157400187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66100981-C-A

157400187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66100981-C-T

157400200-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66100993-T-A

http://identifiers.org/hco/3/GRCh38#157401080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66101873-A-C

157401107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66101900-C-T

157401860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66102804-G-T

157401886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66102824-G-A

157401886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66102824-G-T

157402027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66102954-G-A

157402121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66103050-T-C

157402239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66103165-C-G

http://identifiers.org/hco/3/GRCh38#157402627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66103998-A-C

157402627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66103998-A-G

157402636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66104007-G-A

157402636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66104007-G-C

157402716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66104087-C-T

157402933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66104261-T-C

157403049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66104367-C-T

157403116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66104429-C-T

157405780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -T-A

http://identifiers.org/hco/3/GRCh38#157406032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

157406032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

157406084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66105362-T-A

157406116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66105396-A-G

157406140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66105426-A-G

http://identifiers.org/hco/3/GRCh38#157406418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66105703-C-A

157406418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66105703-C-T

157406690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66105975-G-A

157406702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66105987-G-A

157406904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66106154-T-C

http://identifiers.org/hco/3/GRCh38#157406988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66106253-C-A

157407072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66106328-A-G

157407166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66106407-A-G

157407324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66106573-A-G

157407358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66106607-C-G

http://identifiers.org/hco/3/GRCh38#157407549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66106753-C-A

157407651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66106846-C-T

157407673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66106868-T-C

http://identifiers.org/hco/3/GRCh38#157407866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66107008-A-C

157407884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66107033-A-G

157407995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66107154-C-T

157408028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66107192-C-T

157408029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66107193-G-A

http://identifiers.org/hco/3/GRCh38#157408156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66107298-C-A

157408206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66107346-A-G

157408217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66107358-T-C

157408270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66107424-C-G

157408417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66107780-G-T

157408661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66108387-G-C

157408707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66108431-C-T

157408734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66108458-G-A

157408946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66108710-T-C

157409148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66108851-G-C

157409360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66109229-T-C

157409555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66109454-G-T

http://identifiers.org/hco/3/GRCh38#157409682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66109576-C-A

157409682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66109576-C-G

157409682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66109576-C-T

http://identifiers.org/hco/3/GRCh38#157409970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66109794-C-A

157410023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66109833-A-G

157410033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66109843-C-T

157410104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66109903-A-G

157410246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66110044-A-T

157410268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66110068-C-T

157410291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66110091-G-A

157410416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66110201-C-T

157410436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66110220-T-G

http://identifiers.org/hco/3/GRCh38#157410666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66110453-C-A

157410666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66110453-C-T

http://identifiers.org/hco/3/GRCh38#157410879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66110665-C-A

157412485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66111578-G-C

157412500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

157412542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

http://identifiers.org/hco/3/GRCh38#157413046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66111954-C-A

157413084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66111991-C-T

157413235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66112164-T-C

157413466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66112345-G-A

157413466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66112345-G-T

157413472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66112351-A-G

157413505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66112384-T-G

157413512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66112391-T-C

http://identifiers.org/hco/3/GRCh38#157414096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66113112-A-C

157414096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 66113112-A-G

157414143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66113159-T-A

157414467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66113565-T-C

157414571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66113683-A-G

157414633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66113744-T-C

http://identifiers.org/hco/3/GRCh38#157414635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66113746-C-A

157416385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66114012-T-G

157416602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66114222-T-C

157416866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66114414-G-A

http://identifiers.org/hco/3/GRCh38#157416992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66114513-A-C

http://identifiers.org/hco/3/GRCh38#157417081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66114598-C-A

157417081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66114598-C-T

157417249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66114727-T-C

157417472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66114951-G-A

157417563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66115022-T-G

157417879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66115281-T-C

157417945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66115341-C-G

157420434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66116211-A-G

157420676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66116442-G-T

157421536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66117898-G-A

157421578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66117947-C-T

157421644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66117987-T-C

http://identifiers.org/hco/3/GRCh38#157421707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66118020-C-A

157421794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66118081-G-A

157422117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66118435-G-C

157422233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66118548-T-C

http://identifiers.org/hco/3/GRCh38#157422502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66118809-C-A

http://identifiers.org/hco/3/GRCh38#157422705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66120913-A-C

157422774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66120983-A-G

157422786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66120995-T-A

157428454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 66122964-C-T

http://identifiers.org/hco/3/GRCh38#157428501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66123018-C-A

157428501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66123018-C-T

157428615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66123128-T-C

157428806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66123329-G-T

157429200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66123704-G-T

157429273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66123779-G-A

157429608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66124548-T-C

157429720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66124665-T-C

http://identifiers.org/hco/3/GRCh38#157429745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66124687-A-C

157429745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66124687-A-G

157429782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66124724-T-C

157429955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66124903-T-C

157429974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66124921-A-G

http://identifiers.org/hco/3/GRCh38#157430052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66125035-A-C

157430101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66125083-G-A

157430107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66125089-T-C

157430131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66125113-T-C

http://identifiers.org/hco/3/GRCh38#157430208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66125189-A-C

157430298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66125274-T-C

157430405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66125377-T-C

157436450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66127018-G-C

157436570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66127127-G-A

157436664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66127221-G-C

157436664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66127221-G-T

157436806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66127357-G-T

157436850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66127397-A-G

157436885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 66127430-G-A

157437051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant
orthologous variants: 66127600-C-T

157437091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66127639-T-A

157437220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66127803-A-G

157437405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66127978-G-A

http://identifiers.org/hco/3/GRCh38#157437428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#66128001-C-A

157437428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, undefined
orthologous variants: 66128001-C-T

http://identifiers.org/hco/3/GRCh38#157437507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#66128065-C-A

http://identifiers.org/hco/3/GRCh38#157437565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66128123-C-A

157437601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 66128159-G-A

157437601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 66128159-G-C

157437601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 66128159-G-T

157437641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant
orthologous variants: 66128199-A-G

157437706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 66128264-C-G

http://identifiers.org/hco/3/GRCh38#157437754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#66128312-C-A

157437754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 66128312-C-G

157437754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 66128312-C-T

157437768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 66128326-G-A

157437768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 66128326-G-T

http://identifiers.org/hco/3/GRCh38#157437832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66128390-C-A

157437832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 66128390-C-G

157437832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 66128390-C-T

http://identifiers.org/hco/3/GRCh38#157437839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66128397-C-A

157437839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant
orthologous variants: 66128397-C-G

157437839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 66128397-C-T

157437842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant
orthologous variants: 66128400-G-A

157437842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant
orthologous variants: 66128400-G-C

157437842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, stop_gained
orthologous variants: 66128400-G-T

157437843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant
orthologous variants: 66128401-A-G

157437843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant
orthologous variants: 66128401-A-T

157437859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 66128417-G-A

157437859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 66128417-G-C

157437859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 66128417-G-T

http://identifiers.org/hco/3/GRCh38#157437865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#66128423-C-A

157437865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 66128423-C-G

157437865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 66128423-C-T

157437877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 66128435-G-A

157437877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 66128435-G-T

157437883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 66128441-G-A

157437883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 66128441-G-C

157437883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 66128441-G-T

http://identifiers.org/hco/3/GRCh38#157437905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66128463-C-A

157437905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 66128463-C-T

http://identifiers.org/hco/3/GRCh38#157437949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66128486-C-A

157437949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66128486-C-T

157437950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66128487-G-A

157437950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66128487-G-T

http://identifiers.org/hco/3/GRCh38#157438088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66128554-C-A

http://identifiers.org/hco/3/GRCh38#157438227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66128688-C-A

157438315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66128777-C-T

157438478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66128932-C-T

157438570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66129013-G-C

157438630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66129057-C-T

157438701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66129117-C-G

157438736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66129151-G-A

157438829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66129238-A-G

157438859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66129264-T-C

157438907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66129312-C-T

157439100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66129509-G-T

157439119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66129527-T-C

157439249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66129648-T-A

157439351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66129731-T-G

157439420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66129811-G-A

157440352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66130393-A-G

157440892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66130782-C-T

http://identifiers.org/hco/3/GRCh38#157440996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66130870-C-A

157441244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66131078-C-G

157441244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66131078-C-T

157441847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66131531-A-G

157442071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66131738-G-A

157442194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66131865-T-C

http://identifiers.org/hco/3/GRCh38#157442226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66131897-C-A

157442226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66131897-C-T

157442248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66131919-T-A

157442248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66131919-T-C

157442248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66131919-T-G

157443048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 66132690-T-C

http://identifiers.org/hco/3/GRCh38#157443063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66132706-C-A

157443063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66132706-C-T

157443129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66132760-A-G

157443266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66132894-T-C

157443410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66133048-G-A

157443410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66133048-G-C

157443410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66133048-G-T

http://identifiers.org/hco/3/GRCh38#157443453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66133097-A-C

157443484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66133128-G-A

157443524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66133168-G-T

157443727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66133358-A-G

157443742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66133374-G-T

157443885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66133487-G-A

157444003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, undefined
orthologous variants: 66140853-C-T

157444103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, undefined
orthologous variants: 66140944-G-A

157444125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66140960-G-A

157444165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66140992-C-T

157444235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, undefined
orthologous variants: 66141061-A-G

157444356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66141164-G-A

157444696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66141503-A-G

http://identifiers.org/hco/3/GRCh38#157444834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66141797-A-C

157445044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66141991-T-G

157445283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66142234-G-A

157446044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66142447-C-T

157446065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66142468-A-G

157446174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, undefined
orthologous variants: 66142577-T-C

157446560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66142925-G-A

http://identifiers.org/hco/3/GRCh38#157446591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66142952-A-C

http://identifiers.org/hco/3/GRCh38#157446605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66142966-C-A

157446640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66143007-A-G

157446693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66143063-C-G

157446697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66143068-G-A

157446911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66143283-T-C

157446911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66143283-T-G

157446920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66143292-T-C

157446920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66143292-T-G

http://identifiers.org/hco/3/GRCh38#157446993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66143354-A-C

157447072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66143429-G-T

157447223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, undefined
orthologous variants: 66144074-G-A

157447914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66145015-T-C

157448067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66145137-C-G

157448151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66145227-C-T

157448202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66145279-A-G

157448239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66145316-A-T

157448282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66145359-T-C

157448325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66145402-T-C

157448341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66145418-G-A

157448435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66145510-T-A

157448641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66145715-C-T

http://identifiers.org/hco/3/GRCh38#157450815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66146844-C-A

157451046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66147064-T-C

157451184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66147187-T-C

157451206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66147209-T-G

http://identifiers.org/hco/3/GRCh38#157451523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66147402-C-A

http://identifiers.org/hco/3/GRCh38#157451689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66147546-A-C

157451849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66147699-A-G

157451863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66147713-A-G

157451940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66147777-G-A

157452381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66148214-G-A

157452499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66148299-C-T

157452554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66148350-G-A

http://identifiers.org/hco/3/GRCh38#157452595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66148391-C-A

157452632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66148422-T-G

157452635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66148425-C-T

157452666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66148452-A-G

157452701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66148483-A-G

157452838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66148581-G-A

157452838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66148581-G-T

157452904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66148636-T-A

http://identifiers.org/hco/3/GRCh38#157452950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66148682-C-A

157453327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66149271-T-C

157453404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66149344-T-C

http://identifiers.org/hco/3/GRCh38#157453457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66149396-A-C

157453507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66149433-G-T

157454172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66150053-G-C

157454205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66150089-T-C

157454269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66150151-G-T

157454323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66150205-G-T

http://identifiers.org/hco/3/GRCh38#157459288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66150940-C-A

157459288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66150940-C-T

157459348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66150996-G-C

157459397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66151052-T-C

157459405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66151060-T-G

http://identifiers.org/hco/3/GRCh38#157459427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66151070-C-A

157459427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron variant
orthologous variants: 66151070-C-T

http://identifiers.org/hco/3/GRCh38#157459521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66151158-C-A

157459521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66151158-C-T

157459533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66151170-T-A

157459533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66151170-T-C

http://identifiers.org/hco/3/GRCh38#157459611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66151260-C-A

157459617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66151266-G-A

157459617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66151266-G-T

157459717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66151336-G-A

157459761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66151387-C-G

157459761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66151387-C-T

157459907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66151635-C-T

157459917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66151646-G-A

157459994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66151726-G-A

157459994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66151726-G-C

157460000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66151732-G-C

157460018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66151750-T-G

157460024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66151756-A-G

157460044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66151777-T-G

157460097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66151827-C-T

157460172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 66151890-G-A

157460230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 66151948-T-G

157460382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66152100-T-C

157460416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66152123-T-C

157460419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66152126-C-G

157460419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66152126-C-T

http://identifiers.org/hco/3/GRCh38#157460422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66152129-A-C

157460441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66152148-G-C

157460441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66152148-G-T

157460768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66152422-T-A

157460897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66152532-A-T

157460973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66152594-T-A

157460988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66152609-A-G

157461699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66155581-G-A

157461781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66155663-T-A

157461781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66155663-T-C

157461781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66155663-T-G

157462124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66155934-G-T

157462380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66156152-A-G

157462458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66156216-G-A

157462570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66156295-G-A

157462680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66156385-A-G

157462928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66156719-T-C

157463024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66156805-T-C

http://identifiers.org/hco/3/GRCh38#157463656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66157672-C-A

157463656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66157672-C-T

157464003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66158011-G-A

http://identifiers.org/hco/3/GRCh38#157464055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66158054-A-C

157464368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66159237-T-C

157464411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66159281-A-G

157464461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66159334-G-A

157464537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66159412-G-C

http://identifiers.org/hco/3/GRCh38#157464971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66159835-A-C

157464971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66159835-A-G

157465051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66159907-C-T

157465511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66160644-A-G

157465984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66161074-C-T

157466288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66161428-C-T

157466317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66161456-G-A

157466324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66161463-G-A

157466349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66161489-A-G

157470123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66162108-G-A

157470123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66162108-G-T

157470174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66162163-T-A

157470174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66162163-T-C

157470174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66162163-T-G

157470188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66162177-G-T

http://identifiers.org/hco/3/GRCh38#157470261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66162250-C-A

157470275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66162264-A-G

157470275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66162264-A-T

157470290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66162279-G-T

157470299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66162288-T-G

157470305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66162294-C-G

157470341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 66162330-T-C

157470541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66162535-G-A

157470561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66162555-A-G

http://identifiers.org/hco/3/GRCh38#157470674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66162641-C-A

157470674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66162641-C-G

157470674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66162641-C-T

157470750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66162690-C-T

157470811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66162751-T-C

157470862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66162791-T-C

157471151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66163077-G-A

157471468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66163357-T-C

157471496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66163385-G-T

157471568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66163458-G-A

157471660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66163552-C-G

157471660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66163552-C-T

157471688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66163580-A-T

http://identifiers.org/hco/3/GRCh38#157471707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66163598-A-C

157471707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66163598-A-G

157471707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66163598-A-T

157491452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66167064-G-C

157491601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66167202-T-C

157491775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66167363-A-G

157491782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66167370-A-G

157492281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66167878-A-G

157492285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66167880-A-G

157492359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66167950-A-G

157492441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66168025-C-T

157492596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66168167-T-C

157492812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66169040-T-G

157493054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66169270-C-G

157493239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66169436-T-C

157493281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66169487-C-T

157493326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66169530-T-G

157493706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66169869-A-G

157493948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66170116-A-G

157494097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66170251-A-G

157494276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66170420-T-C

157494348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66170478-G-A

157494441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66170575-C-T

157494481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66170615-C-T

http://identifiers.org/hco/3/GRCh38#157494674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66170790-A-C

157494826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66170942-C-T

157495128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66171225-A-G

157495173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66171265-G-A

157495173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66171265-G-T

157495199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66171290-C-T

http://identifiers.org/hco/3/GRCh38#157495323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66171414-C-A

157495362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66171447-T-C

157495433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66171514-T-C

157495453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66171534-T-C

http://identifiers.org/hco/3/GRCh38#157495526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66171607-C-A

157495526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66171607-C-T

http://identifiers.org/hco/3/GRCh38#157495551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66171634-C-A

157495552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66171635-A-T

157495607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66171701-T-G

157495790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66171908-T-C

157496266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66172353-A-T

157496436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66172522-G-A

157496604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66172694-C-G

157496665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66172753-G-A

157496686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66172774-C-T

157496765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66172859-C-T

157496832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66172916-A-G

157496912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66196649-A-G

157497293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66197154-T-C

http://identifiers.org/hco/3/GRCh38#157497295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66197156-A-C

157497316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66197177-C-G

157497325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66197186-C-T

157497342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66197205-G-A

157497362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66197224-T-C

157497369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66197231-C-T

157497389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66197253-A-T

http://identifiers.org/hco/3/GRCh38#157497406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66197271-A-C

157497553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66197416-T-C

157497567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66197434-T-C

http://identifiers.org/hco/3/GRCh38#157497649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66197509-C-A

157497649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66197509-C-T

157497698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66197554-C-T

157497743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66197589-T-A

157497743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66197589-T-C

157497743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66197589-T-G

157497773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66197618-C-G

157497780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66197625-C-T

157497819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66197663-A-T

157498870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66199358-G-A

http://identifiers.org/hco/3/GRCh38#157499233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#66199589-C-A

157499326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66199700-C-T

157499398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 66199762-C-T

157499487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 66199838-G-T

157499534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 66199879-G-T

157499537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 66199882-G-A

157499537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 66199882-G-T

157499540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 66199885-G-A

157499540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 66199885-G-T

157499752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 66200072-G-T

157499753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 66200073-G-T

157499837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 66200156-C-G

157499954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66200229-C-G

157499954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66200229-C-T

http://identifiers.org/hco/3/GRCh38#157500213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66200864-C-A

157500793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66201446-G-A

157500793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66201446-G-C

157501102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66201915-A-G

157501332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66202148-C-G

157501500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66202314-G-C

157501531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66202332-G-T

157501539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66202340-C-T

157501884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66202667-C-T

157502151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 66202939-T-A

157502288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66203072-T-G

157502573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66203356-T-C

157502573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66203356-T-G

http://identifiers.org/hco/3/GRCh38#157502939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66203690-A-C

157503013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66203753-C-T

157503095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66203837-T-G

157503230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66203977-G-T

157503239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66203986-T-C

157503349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66204097-G-T

http://identifiers.org/hco/3/GRCh38#157503388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66204136-C-A

157503388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66204136-C-T

http://identifiers.org/hco/3/GRCh38#157504257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66204947-A-C

157504319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66204996-A-G

http://identifiers.org/hco/3/GRCh38#157504799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66205415-C-A

http://identifiers.org/hco/3/GRCh38#157504888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66205570-C-A

157505013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66205693-G-A

157505183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66205832-G-A

http://identifiers.org/hco/3/GRCh38#157505473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66205939-C-A

157505535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66205982-G-A

157506148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66206462-C-T

157506269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66206572-T-C

157506570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66206874-A-G

157506635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66206939-T-A

157508246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66208736-T-C

http://identifiers.org/hco/3/GRCh38#157508250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66208740-C-A

157508250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66208740-C-G

157508250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66208740-C-T

157508447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66208919-G-A

157508536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66209016-C-G

157508546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66209026-C-G

157508751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66209199-G-A

157508767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66209217-T-C

157508900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66209341-A-G

157508942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66209380-A-G

157508993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66209433-T-C

157509001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66209441-T-C

157509036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66209477-A-T

157520583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66221942-A-G

157520702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66222062-A-G

157520708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66222440-C-T

157521244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66222973-C-T

157521262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66222991-T-C

157521289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66223018-T-C

http://identifiers.org/hco/3/GRCh38#157521435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66223155-C-A

157521435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66223155-C-T

157522531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66224410-G-A

http://identifiers.org/hco/3/GRCh38#157522670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66224544-A-C

157522708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66224579-C-T

157522848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66224717-T-A

157522915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66224784-G-A

157522984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66224855-G-A

157522984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66224855-G-T

157523380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66224884-C-T

http://identifiers.org/hco/3/GRCh38#157523709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66225185-A-C

157523709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66225185-A-G

157523709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66225185-A-T

http://identifiers.org/hco/3/GRCh38#157523716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66225192-A-C

157523716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66225192-A-G

157523716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66225192-A-T

157523998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66225462-G-A

157523998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66225462-G-C

157524216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66225682-T-C

157524336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66225807-T-C

157524391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66225869-T-C

157524434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66225908-A-G

157524442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66225916-A-T

157527061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66232920-A-G

157527061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66232920-A-T

157527091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66232935-T-C

157527154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66232998-G-A

157527154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66232998-G-T

http://identifiers.org/hco/3/GRCh38#157527655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66233508-A-C

157527655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66233508-A-G

157527657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66233517-T-C

157527667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66233527-A-G

157527782-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66233640-A-T

157528015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66233876-G-T

157528425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66234290-G-A

http://identifiers.org/hco/3/GRCh38#157528558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66234419-C-A

157528970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66235594-T-A

157528974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66235598-C-G

157528974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66235598-C-T

157529044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66235659-G-A

157529151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66235732-C-T

157529163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66235744-A-G

157529355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66235924-G-T

157529956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66236765-C-T

157530405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66237021-C-T

157530599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66237717-A-G

157530645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66237759-G-A

http://identifiers.org/hco/3/GRCh38#157530691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66237770-C-A

157530691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66237770-C-T

157530783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 66237850-G-A

157531050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66238122-A-T

157531103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66238158-G-T

157531334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66238241-C-T

157531359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66238282-C-T

157531530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66238446-T-G

157531626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66238548-C-G

157531626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66238548-C-T

157531756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66238648-G-C

157531805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66238696-T-A

157531805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66238696-T-C

157532200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66238982-T-C

157532268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66239038-C-T

157532387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66239132-T-C

157532477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66239216-C-G

157532640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 66239369-G-A

157532640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 66239369-G-C

157532640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 66239369-G-T

157532674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66239397-T-G

157532755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66239460-T-C

http://identifiers.org/hco/3/GRCh38#157532844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66239546-C-A

157533364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66240067-T-C

157533385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66240083-T-C

157533421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66240119-G-A

157533449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66240137-C-T

157533452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25735
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66240140-A-G