15778342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12352221-C-T

15778367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12352255-T-A

15778398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12352285-A-G

15778498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12352410-T-C

http://identifiers.org/hco/10/GRCh38#15778687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12352571-C-A

15778691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12352575-A-G

15778888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12352768-T-G

15778937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12352810-G-C

15778937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12352810-G-T

http://identifiers.org/hco/10/GRCh38#15779177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12353047-C-A

15779177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12353047-C-T

15779178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12353048-A-G

15779237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12353111-T-A

http://identifiers.org/hco/10/GRCh38#15779279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12353141-C-A

15779279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12353141-C-T

15779294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12353149-A-G

15779398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12353261-C-T

15779553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12353414-C-G

15779553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12353414-C-T

15779637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12353464-T-C

15779637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12353464-T-G

15779703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12353531-G-A

15779849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12353663-T-G

15780045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12353810-G-A

15780187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12353953-G-C

15780841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12354528-T-A

15780977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12354664-T-C

15781037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12354709-T-A

15781602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12355192-G-A

15781612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12355202-T-C

15781614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12355204-A-G

15782025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12355614-T-C

15782025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12355614-T-G

http://identifiers.org/hco/10/GRCh38#15782031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12355619-C-A

15782031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12355619-C-T

http://identifiers.org/hco/10/GRCh38#15782140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12355725-C-A

15782140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12355725-C-T

15782321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12355910-T-C

15782329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12355916-G-C

15782329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12355916-G-T

15782336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12355923-G-A

15782336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12355923-G-T

15782425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12355986-G-A

15782425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12355986-G-T

15782583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12356128-C-T

http://identifiers.org/hco/10/GRCh38#15782954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12356301-C-A

15783058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12356410-T-C

15783119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12356465-T-C

15783172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12356515-G-A

15783653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12356775-A-G

15783746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12356845-A-T

15786633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12360160-C-T

http://identifiers.org/hco/10/GRCh38#15786642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12360169-A-C

15786642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12360169-A-G

15786642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12360169-A-T

15786942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12360484-T-C

15786976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12360518-G-A

http://identifiers.org/hco/10/GRCh38#15787316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12360804-A-C

15787438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12360930-A-G

15787462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12360954-G-A

15787504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12360996-C-T

15789027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12361518-G-T

15789072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12361570-T-C

http://identifiers.org/hco/10/GRCh38#15789102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12361601-C-A

15789102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12361601-C-T

http://identifiers.org/hco/10/GRCh38#15789415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12361864-A-C

15789415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12361864-A-G

http://identifiers.org/hco/10/GRCh38#15789437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12361886-C-A

15789437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12361886-C-T

15789503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12361951-T-C

http://identifiers.org/hco/10/GRCh38#15789599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12362060-C-A

15789599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12362060-C-G

15789599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12362060-C-T

15789644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12362102-C-T

15789995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12365786-T-C

15790024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12365816-A-G

15790046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12365824-T-C

15790317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12366012-G-A

15790424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12366118-A-G

15790424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12366118-A-T

15790575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12366269-T-C

15793427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12366767-A-G

15795605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12368621-A-G

15796032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12369205-A-G

15796068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12369234-T-C

15796242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12369398-G-A

15796242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12369398-G-T

15796250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12369404-G-T

15796288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12369431-T-C

15796348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12369492-C-T

15796537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12369686-T-C

15796875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12369986-A-G

15797326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12370481-A-G

15797465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12370578-T-C

15797482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12370595-C-T

15803809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12375915-A-G

15803872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12375975-G-C

15803872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12375975-G-T

15804379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12376646-A-G

15804598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12376841-T-C

15805048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12377302-C-T

15807517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12377690-A-G

15807861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12378033-G-C

15807901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12378066-G-C

http://identifiers.org/hco/10/GRCh38#15808258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12378400-A-C

15808394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12378597-C-T

15808498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12378686-C-T

15808580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12378746-G-T

15808691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12378830-G-A

http://identifiers.org/hco/10/GRCh38#15808816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12379031-C-A

http://identifiers.org/hco/10/GRCh38#15808955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12379176-C-A

15808955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12379176-C-T

15809309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12379523-A-T

15809318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12379532-G-T

15809562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12379790-T-C

15812813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12380717-A-G

http://identifiers.org/hco/10/GRCh38#15812889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12380793-A-C

15812889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12380793-A-G

15812963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12380865-T-C

15813062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12384615-A-G

15813084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12384637-T-A

15813172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12384716-T-C

15813284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12384828-G-C

http://identifiers.org/hco/10/GRCh38#15813648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12385157-C-A

15813648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12385157-C-T

15814100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12385628-C-T

15814133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12385661-T-A

15814174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12385700-C-T

15815284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12386057-G-A

15815332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12386091-A-G

15815592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12386294-A-G

15815594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12386295-G-A

15815642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12386346-C-G

15815642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12386346-C-T

15815783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12386437-A-T

15815798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12386452-T-C

15815914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12386560-T-C

15815927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12386573-G-C

15816716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12386793-A-G

15817005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12387087-G-T

http://identifiers.org/hco/10/GRCh38#15817052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12387102-A-C

http://identifiers.org/hco/10/GRCh38#15817070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12387121-C-A

15817174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12387223-T-C

15817247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12387258-T-A

15817689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12387387-T-C

15817692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12387390-C-T

15817701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12387399-G-C

15817701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12387399-G-T

http://identifiers.org/hco/10/GRCh38#15817758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12387437-C-A

15817760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12387439-A-G

http://identifiers.org/hco/10/GRCh38#15817858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12387537-C-A

15817952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12387621-G-A

15818136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12387775-G-A

15818136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12387775-G-T

15818137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12387776-A-T

http://identifiers.org/hco/10/GRCh38#15818195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12387833-A-C

15818262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12387862-G-C

15818319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12387932-A-G

15818407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12388006-G-T

15818561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12388149-C-T

15818874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12388763-G-A

15819278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12389150-T-C

15819478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12389326-T-C

15819574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12389420-C-T

15820459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12390386-C-T

15820460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12390387-C-T

15820495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12390418-T-A

15820499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12390422-T-C

15820514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12390437-G-A

15820514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12390437-G-C

15820650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12390558-G-A

15820732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12390636-A-G

15821459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12391244-T-C

15821513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12391291-T-C

15821513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12391291-T-G

15821563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12391343-G-T

15821629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12391396-T-C

15821741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12391504-A-G

http://identifiers.org/hco/10/GRCh38#15821975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12391978-A-C

15821975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12391978-A-G

15824521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12393861-T-C

15824723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12394056-C-T

http://identifiers.org/hco/10/GRCh38#15824907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12394357-C-A

15831449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12399123-A-G

http://identifiers.org/hco/10/GRCh38#15831454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12399128-C-A

15832320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12399562-G-C

http://identifiers.org/hco/10/GRCh38#15832407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12399618-C-A

15832805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12399949-T-A

15833045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12400417-T-A

15833070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12400441-C-T

15833190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12400544-T-A

15833250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12400599-A-G

http://identifiers.org/hco/10/GRCh38#15833307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12400657-A-C

15833339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12400686-G-C

15833748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401109-A-G

15833810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401163-T-C

15833810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401163-T-G

15834032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401796-T-A

15834032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401796-T-C

15834057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401821-T-C

15834083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401847-G-A

15834120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401882-C-T

http://identifiers.org/hco/10/GRCh38#15834358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12402122-A-C

15834531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12402293-T-A

15834531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12402293-T-C

15834531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12402293-T-G

15834572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12402333-G-A

15834572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12402333-G-T

http://identifiers.org/hco/10/GRCh38#15834696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12402434-C-A

15834696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12402434-C-G

15834819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12402529-G-A

15834831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12402541-C-T

15835123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12402844-T-G

15835460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12403116-A-G

15835706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12403352-C-T

15835781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12403431-T-C

15836040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12403702-T-C

http://identifiers.org/hco/10/GRCh38#15836153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12403799-A-C

15836153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12403799-A-G

http://identifiers.org/hco/10/GRCh38#15836184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12403829-C-A

15836211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12403855-C-T

15836235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12403879-C-T

15836321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12403936-A-G

15836444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12404115-T-C

http://identifiers.org/hco/10/GRCh38#15836570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12404219-C-A

15836760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12404409-G-A

15837087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12404737-A-G

15837088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12404738-G-T

http://identifiers.org/hco/10/GRCh38#15837095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12404745-A-C

15837436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12405055-T-C

15837436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12405055-T-G

15837480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12405102-C-T

15837567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12405187-A-G

15837606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12405221-A-G

15837674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12405285-A-T

http://identifiers.org/hco/10/GRCh38#15837999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12405607-A-C

15838050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12405657-T-C

15838123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12405731-T-C

http://identifiers.org/hco/10/GRCh38#15838150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12405758-C-A

15838150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12405758-C-G

15838150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12405758-C-T

http://identifiers.org/hco/10/GRCh38#15838419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12406026-C-A

15839033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12406552-T-A

15839195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12406711-T-G

15839553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12407045-T-G

15839612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12407125-G-A

http://identifiers.org/hco/10/GRCh38#15839635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12407148-A-C

15839684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12407191-C-T

15839974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12407470-G-T

15839979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12407475-G-A

http://identifiers.org/hco/10/GRCh38#15840473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12407912-C-A

15840473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12407912-C-G

15840610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12408051-G-A

15840674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12408101-C-T

15840766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12408192-C-G

15841032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12408446-G-A

15841125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12408525-C-T

15841222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12408634-T-A

15841619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12408999-A-G

15841939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12409277-A-G

15842208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12409560-A-G

http://identifiers.org/hco/10/GRCh38#15842294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12409634-A-C

15842310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12409640-G-A

15842312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12409642-A-G

15842378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12409700-T-C

15842487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12409791-T-G

http://identifiers.org/hco/10/GRCh38#15842888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12410163-C-A

15843048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12410476-A-G

15843363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12410815-A-G

15843372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12410824-C-G

15843372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12410824-C-T

15843384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12410836-C-T

15843428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12410875-G-T

15843553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12410996-C-G

15843553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12410996-C-T

15843752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12411685-C-G

15843835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12411743-T-C

http://identifiers.org/hco/10/GRCh38#15844008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12411888-C-A

15844160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412026-T-C

15844160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412026-T-G

15844375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412240-T-A

15844804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412652-T-C

15845141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412969-T-C

15845307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413116-G-A

http://identifiers.org/hco/10/GRCh38#15846275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12413484-C-A

15846275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413484-C-G

15846349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413553-T-G

15846369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413570-C-G

15846465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413665-T-C

http://identifiers.org/hco/10/GRCh38#15847734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12414684-C-A

15847736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12414686-T-A

15847929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12414877-C-G

15847963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12414910-G-A

15847963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12414910-G-C

15847963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12414910-G-T

http://identifiers.org/hco/10/GRCh38#15848034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12414976-C-A

15848035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12414977-T-G

15848120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12415062-C-T

15848830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12415742-A-G

15849231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12416162-A-G

15851624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12417320-T-C

15851733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12417420-A-G

15852076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12417699-T-C

15852218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12417795-T-C

15852370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 12417938-G-A

15852453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12418013-A-G

15852620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12418181-G-A

15852661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12418208-T-A

15855440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12419983-T-G

15855632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12420171-A-G

15855937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12420460-T-A

15856010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12420533-G-A

15856010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12420533-G-C

15856328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12420821-A-T

15856333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12420826-G-A

15856333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12420826-G-T

http://identifiers.org/hco/10/GRCh38#15856453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12420954-A-C

http://identifiers.org/hco/10/GRCh38#15856584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12421069-C-A

15857225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12421625-T-C

15857273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12421671-G-A

15857581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12421882-C-T

15857742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422400-T-G

http://identifiers.org/hco/10/GRCh38#15857785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12422446-C-A

15857785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422446-C-G

15857916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12422566-C-T

15859645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422809-A-G

15859756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422918-G-A

15859822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422980-C-G

http://identifiers.org/hco/10/GRCh38#15860109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12423844-C-A

15860109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12423844-C-T

http://identifiers.org/hco/10/GRCh38#15860131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12423885-C-A

15860131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12423885-C-T

http://identifiers.org/hco/10/GRCh38#15860276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12424040-C-A

15860334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12424101-G-C

15860334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12424101-G-T

http://identifiers.org/hco/10/GRCh38#15860398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12424166-C-A

15860398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12424166-C-T

15860440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12424201-G-A

15860440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12424201-G-C

15860452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12424213-G-A

15860452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12424213-G-C

http://identifiers.org/hco/10/GRCh38#15860471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#12424230-C-A