17753407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11316442-C-G

17753672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11316241-C-T

17753786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11316151-C-T

17753790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11316140-G-A

17753799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11316131-G-A

17753799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11316131-G-T

17753920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11315997-G-A

17753941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11315976-G-A

17753941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11315976-G-T

17753956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11315959-G-T

http://identifiers.org/hco/2/GRCh38#17754039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#11315894-C-A

17754049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11315884-T-C

http://identifiers.org/hco/2/GRCh38#17754379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11315553-C-A

http://identifiers.org/hco/2/GRCh38#17754532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11315520-C-A

17754532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11315520-C-T

17754727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11315430-T-A

17754727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11315430-T-C

17754816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11315328-A-G

17754841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11315303-T-C

http://identifiers.org/hco/2/GRCh38#17754942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#11315210-C-A

17754942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11315210-C-G

17754942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11315210-C-T

17755150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11315003-G-T

17755249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11314898-C-G

17755271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11314876-G-A

17755271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11314876-G-T

17755321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11314843-C-G

17755348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11314804-A-G

17755626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11314559-A-G

17755954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11314257-G-A

17755980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11314228-A-G

17755980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11314228-A-T

17756022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11314197-T-C

17756184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11314080-T-G

17756238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11314037-A-G

17756353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11313960-C-T

17758323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 11313777-G-A

17758323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 11313777-G-T

17758325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 11313775-T-A

17758325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 11313775-T-C

17758386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11313714-C-G

17758387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11313713-T-G

17759162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11313170-G-A

17759288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11313053-G-A

17759351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11312990-T-C

http://identifiers.org/hco/2/GRCh38#17759908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11312606-A-C

17759939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11312571-C-G

17760046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant
orthologous variants: 11312464-G-A

17760046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant
orthologous variants: 11312464-G-T

17760061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant
orthologous variants: 11312449-A-G

17760061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant
orthologous variants: 11312449-A-T

17760076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant
orthologous variants: 11312434-A-G

17760076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant
orthologous variants: 11312434-A-T

http://identifiers.org/hco/2/GRCh38#17760123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11312387-C-A

17760123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron variant
orthologous variants: 11312387-C-G

17760123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron variant
orthologous variants: 11312387-C-T

17760138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron variant
orthologous variants: 11312371-A-G

17760138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron variant
orthologous variants: 11312371-A-T

http://identifiers.org/hco/2/GRCh38#17760147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11312362-C-A

17760147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron variant
orthologous variants: 11312362-C-G

17760147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron variant
orthologous variants: 11312362-C-T

17760216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron variant
orthologous variants: 11312308-G-A

17760216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron variant
orthologous variants: 11312308-G-T

17761329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron variant
orthologous variants: 11311133-G-A

17761706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11310781-A-G

17761708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11310779-G-A

17761708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11310779-G-T

17761726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11310763-G-T

17761925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11310573-A-G

17761947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11310551-G-A

17761947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11310551-G-T

17762338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11310012-A-G

17762429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11309924-G-A

17762429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11309924-G-T

17762491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11309759-G-T

17762736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11309475-G-A

17763242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11308902-T-C

17763287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11308859-A-G

17763554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11308587-T-C

17763760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11308383-C-T

17764103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307933-C-T

17764205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307821-G-A

17764776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307111-G-A

17764776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307111-G-T

17764786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307103-A-T

17764817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307071-A-G

17764829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307059-G-A

17764829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307059-G-T

17764877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307029-C-G

17764877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307029-C-T

17764909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11307001-C-G

17764909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11307001-C-T

17764939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11306971-G-C

17764975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11306935-A-G

17765008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11306902-A-G

17765059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11306851-A-G

17765122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11306783-T-C

17765123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11306782-T-A

http://identifiers.org/hco/2/GRCh38#17766502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11305329-C-A

17766502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11305329-C-T

17766747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11305111-T-A

17766764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11305093-T-C

17766810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11305026-A-G

17766910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11304845-G-A

17766912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11304843-A-T

17767066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11304705-T-C

17768724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11304437-C-T

http://identifiers.org/hco/2/GRCh38#17768821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11304340-A-C

17768821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11304340-A-G

17768821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11304340-A-T

17768841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11304321-T-C

http://identifiers.org/hco/2/GRCh38#17768847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11304315-C-A

17769218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11304036-T-C

17769219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11304035-A-G

17769944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11303462-A-G

http://identifiers.org/hco/2/GRCh38#17770110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11303306-A-C

17770360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11303066-T-C

17770420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11303008-A-G

17770888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11302334-G-A

17770954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11302307-T-C

17770975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11302286-A-G

http://identifiers.org/hco/2/GRCh38#17771020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11302247-C-A

17771029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11302238-A-T

17771236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 11302051-C-T

17771278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11302012-T-C

17771292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11301998-G-A

17771414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11301913-T-C

17772142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11301296-G-T

17772150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11301288-G-T

17772293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11301155-C-T

17772388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11301081-C-G

17772469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11301011-G-A

17772525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300969-T-G

17772553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300942-T-C

17772593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300903-A-G

17772608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300888-T-G

17772635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 11300862-T-G

17772708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11300789-G-A

http://identifiers.org/hco/2/GRCh38#17772753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11300744-C-A

17772753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 11300744-C-T

http://identifiers.org/hco/2/GRCh38#17772759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11300738-A-C

http://identifiers.org/hco/2/GRCh38#17772805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11300694-A-C

17772805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300694-A-G

http://identifiers.org/hco/2/GRCh38#17772973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11300207-C-A

17772973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300207-C-G

17772987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300188-A-G

17773026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300151-T-A

17773026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300151-T-G

17773033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300144-G-A

17773261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11299167-G-T

17773305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11299123-T-C

http://identifiers.org/hco/2/GRCh38#17773509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11298909-A-C

17773514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11298904-T-C

17773805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11298715-C-T

17773976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11298628-G-C

17774073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11298538-G-A

17774204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11298412-T-A

17774204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11298412-T-C

17774204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11298412-T-G

17774239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11298376-A-G

17774292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11298323-G-A

17774292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 11298323-G-T

17774337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11298278-A-G

17777466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11297092-A-G

17777565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11297005-A-G

17777577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296993-C-T

17777604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296966-G-C

17777871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296472-G-A

17777901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296442-T-C

17777963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296388-T-C

17777963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296388-T-G

17778078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296273-T-C

17778080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296271-A-G

http://identifiers.org/hco/2/GRCh38#17778118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11296234-C-A

17778544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296152-T-C

17778580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296119-A-G

17778670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296035-T-G

http://identifiers.org/hco/2/GRCh38#17778691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11296014-C-A

17780008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11293302-G-A

17780015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11293295-T-C

17780125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11293185-A-G

17780131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11293179-G-A

17780131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11293179-G-T

http://identifiers.org/hco/2/GRCh38#17780153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11293166-A-C

17780153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11293166-A-G

17780163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11293158-G-A

17780163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11293158-G-T

http://identifiers.org/hco/2/GRCh38#17780175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11293146-C-A

17780175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11293146-C-T

17780239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11293096-A-G

17780244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11293092-T-C

http://identifiers.org/hco/2/GRCh38#17780269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11293067-C-A

17780269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11293067-C-T

17780382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292848-T-G

17780607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292589-T-C

17780742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11292448-G-A

17780742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11292448-G-T

17780884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11292306-G-T

17780894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11292296-A-G

17780959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11292231-C-T

17780983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 11292207-G-T

17781134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11292074-C-G

17781172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11292039-A-T

17781191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11292020-T-G

17781207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11292004-T-G

17781213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11291998-A-G

17781264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11291947-T-C

17781290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291921-T-A

17781290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291921-T-C

http://identifiers.org/hco/2/GRCh38#17781291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11291920-C-A

17781291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11291920-C-T

17781362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291852-C-T

17781423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11291791-T-C

17781454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291766-T-C

17781455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291765-A-G

17781459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11291761-A-G

http://identifiers.org/hco/2/GRCh38#17781470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11291750-C-A

17781470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291750-C-G

17781470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291750-C-T

17781575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291639-A-G

17781647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291567-A-G

17781655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291559-T-C

http://identifiers.org/hco/2/GRCh38#17781854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11291360-A-C

17781854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291360-A-G

17781854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291360-A-T

17781902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 11291312-T-G

17781979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11291234-T-C

17781983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11291230-A-G

17781983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11291230-A-T

17782117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11290980-A-G

17782118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11290979-A-G

17782157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11290939-T-C

17782695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11290340-G-A

17782719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11290313-C-T

17782864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11290157-G-A

17784532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11287047-T-C

http://identifiers.org/hco/2/GRCh38#17784560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11287019-C-A

17784560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11287019-C-T

17784635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11286945-A-G

17784635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11286945-A-T

17784801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11286782-C-T

17785278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11286428-T-C

17785345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11286367-G-T

17785478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11286249-T-A

http://identifiers.org/hco/2/GRCh38#17785507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11286218-C-A

17785508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11286217-A-G

17785564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11286162-T-C

17786056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11286041-A-G

17786201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11285887-G-T

17786241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11285856-A-G

17786241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11285856-A-T

17786277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11285823-C-T

17786319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11285778-A-G

17786379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11285725-A-G

17786394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11285710-A-G

17786411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11285689-G-T

17786735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283548-T-C

17786857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283439-G-A

17786857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283439-G-T

http://identifiers.org/hco/2/GRCh38#17786875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11283423-C-A

17786909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283394-T-C

17786944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283364-A-G

17786944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283364-A-T

http://identifiers.org/hco/2/GRCh38#17786971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11283337-C-A

17786971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283337-C-T

http://identifiers.org/hco/2/GRCh38#17786974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11283334-C-A

17786974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283334-C-T

http://identifiers.org/hco/2/GRCh38#17786998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11283321-C-A

17787076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283235-T-C

17787091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283222-T-C

http://identifiers.org/hco/2/GRCh38#17787160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11283172-C-A

17787160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283172-C-T

17787167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283168-A-T

http://identifiers.org/hco/2/GRCh38#17787369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11283053-C-A

17787372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283050-C-T

http://identifiers.org/hco/2/GRCh38#17787518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11282917-C-A

17787765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11282845-A-G

17787959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11282807-T-C

17787967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11282795-G-T

17788029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11282738-T-C

17788081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11282678-C-T

17788178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11282592-T-A

17788356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11282403-T-G

http://identifiers.org/hco/2/GRCh38#17788612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11282168-C-A

17788663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11282055-T-A

17788667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11282051-G-C

17788902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11281902-A-T