http://identifiers.org/hco/9/GRCh38#112750695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#59805813-C-A

112750695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59805813-C-G

112750695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59805813-C-T

112750808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59805924-G-T

112750811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59805927-G-A

112750811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59805927-G-T

112750868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59805980-G-A

112750880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59805990-G-A

112750918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59806017-G-T

http://identifiers.org/hco/9/GRCh38#112751112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59806180-C-A

112751112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59806180-C-T

112751238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59806295-C-T

112751508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59806593-G-A

112751702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59806790-G-A

112751856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59806940-G-A

112751856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59806940-G-C

112752114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59807202-C-T

112752149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59807247-C-T

112752779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59807662-T-C

112752885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59807751-C-T

112752904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59807770-A-T

http://identifiers.org/hco/9/GRCh38#112752983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59807804-C-A

112752998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59807819-A-G

112753077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59807897-G-A

112753077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59807897-G-C

112753097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59807917-G-A

112753223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59808175-T-G

112754056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59808891-T-C

112760346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59816106-G-A

112760354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59816098-A-G

112760538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59815898-G-A

112760538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59815898-G-C

112760615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59815723-G-T

112761104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59815121-G-A

112761642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59815023-A-T

112761714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59814955-C-G

112761714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59814955-C-T

112761715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59814954-G-A

112761804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59814871-A-G

112762220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59814400-A-T

112762235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59814385-T-A

112762242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59814363-G-C

112762278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59814318-T-C

112762367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59814236-G-A

112765509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59820888-C-T

112765816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59821245-C-T

112766277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59821787-A-T

112766294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59821803-T-A

112766364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59821874-C-T

112766375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59821882-G-C

112766375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59821882-G-T

112772445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59831552-G-A

112772779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59832729-C-G

112772834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59832778-A-T

112772905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59832848-A-T

112772921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59832864-A-G

112772954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59832895-T-G

112773193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59833114-T-C

http://identifiers.org/hco/9/GRCh38#112773331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59833218-A-C

112773806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59835003-C-T

112773879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59835090-G-A

112773948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59835162-A-G

112773948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59835162-A-T

112773988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59835204-T-A

112774039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59835254-C-T

112780655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59838606-A-G

112781044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59838914-C-T

112782539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59841142-T-A

112783095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59841663-A-G

112783142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59841712-A-T

112783290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59841842-C-G

112784275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59842356-G-A

112784278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59842359-T-A

112784428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59842487-C-G

112784452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59842511-C-T

112784763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59842768-G-A

112784802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59842843-C-G

112784802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59842843-C-T

112784837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59842889-T-C

112784893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59842946-T-G

112786020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59843554-T-C

112786493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59843674-C-T

112786956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59844600-T-G

http://identifiers.org/hco/9/GRCh38#112786984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59844628-A-C

112787023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59844671-C-T

112787108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59844739-G-A

112787331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59844919-T-C

112787348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59844936-T-C

112787525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59845101-G-A

112788797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59846972-T-A

112789266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59847425-T-C

112789336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59847495-G-A

112789806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59847925-T-C

http://identifiers.org/hco/9/GRCh38#112789811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59847930-C-A

112789927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59848044-A-G

112790012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59848129-C-T

112790059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59848173-C-T

112790417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59848520-G-A

112790418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59848521-G-A

112790466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59848566-G-A

112790474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59848574-A-G

112790651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59848743-A-G

112792755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59849800-T-C

112792978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59849974-C-T

112793007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59849997-G-T

112793085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59850084-T-A

112793653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59850601-C-G

112793842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59850763-T-C

112794498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59851253-A-G

112794549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59851306-C-T

112794835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59851573-G-A

112795017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59851745-C-T

112795569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59854596-C-T

112795728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59854713-A-G

112795957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59855116-A-G

http://identifiers.org/hco/9/GRCh38#112796785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59856085-C-A

112796785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59856085-C-T

112797006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59856235-C-G

112804630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59857315-A-T

112804657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59857342-G-A

112804657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59857342-G-T

112804662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59857347-G-A

112804662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59857347-G-C

112804662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59857347-G-T

112804979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59857645-T-C

112804979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59857645-T-G

112804984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59857650-T-C

112804996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59857662-G-A

112804999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59857665-G-T

112805027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59858095-T-C

112805060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59858138-G-A

112805060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59858138-G-T

112805061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59858139-T-C

112805092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59858170-A-G

112805179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59858238-G-A

112806215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59858897-A-G

112806215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59858897-A-T

112806332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59858991-A-G

112806755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59859792-A-G

112806863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59859877-A-G

112806899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59859912-A-G

112806986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59860010-T-A

http://identifiers.org/hco/9/GRCh38#112807568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59860158-A-C

112807821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59860431-C-G

112808312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59861626-T-C

112810094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59864145-T-G

112810135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59864186-G-A

112810193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59864249-A-G

112815040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59866061-C-T

112815041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59866062-G-A

112815099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59866118-A-T

112815107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59866126-T-C

112815220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59866392-A-G

112816510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59866728-T-G

112816523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59866741-T-G

http://identifiers.org/hco/9/GRCh38#112816573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59866778-C-A

112816573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59866778-C-T

http://identifiers.org/hco/9/GRCh38#112816585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59866786-C-A

112816585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59866786-C-T

112816594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59866795-T-C

112816773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59866971-T-G

112816785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59866983-A-T

112816978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59867156-T-A

112816978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59867156-T-C

112816983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59867161-A-G

112816983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59867161-A-T

112817146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59867558-C-G

112817146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59867558-C-T

112817324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59867738-G-T

112817383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59867796-G-A

http://identifiers.org/hco/9/GRCh38#112817397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59867845-C-A

112817397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59867845-C-G

112817397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59867845-C-T

112817592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59868125-G-A

http://identifiers.org/hco/9/GRCh38#112817642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59868175-C-A

112817642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59868175-C-T

http://identifiers.org/hco/9/GRCh38#112817646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59868179-C-A

112817646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59868179-C-T

http://identifiers.org/hco/9/GRCh38#112817846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59868378-C-A

http://identifiers.org/hco/9/GRCh38#112817847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59868379-A-C

112817847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59868379-A-G

112817955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59868477-C-G

112817955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59868477-C-T

112818744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59870217-C-T

112818935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59870394-T-G

112819161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59870625-A-G

http://identifiers.org/hco/9/GRCh38#112819214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59870668-A-C

112819214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59870668-A-G

112819215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59870669-T-C

112819293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59870688-G-A

112819293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59870688-G-T

112819712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59870857-C-T

112819753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59870880-A-G

112820019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59871042-C-G

112820123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59871149-G-T

112820326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59871332-A-G

112820449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59871461-A-G

112823405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59874894-C-T

112823424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59874913-A-G

112823527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59875010-G-A

112823557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59875044-T-C

http://identifiers.org/hco/9/GRCh38#112824065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59875815-A-C

112829919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59877890-G-C

112830200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59878158-A-G

http://identifiers.org/hco/9/GRCh38#112830338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59878288-A-C

112830341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59878291-T-A

112830341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59878291-T-C

112830781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59879278-T-G

http://identifiers.org/hco/9/GRCh38#112830922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59879418-C-A

112830922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59879418-C-T

112831592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59880745-C-G

112831733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59880879-G-C

112832118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59881264-G-T

112832481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59881507-T-A

112832483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59881509-T-A

112832483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59881509-T-G

112835583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59883761-C-G

112835664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59883839-A-G

112835664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59883839-A-T

112835720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59883898-C-T

112835787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59883960-C-T

112835812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59883985-G-A

http://identifiers.org/hco/9/GRCh38#112836147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59884929-C-A

112836147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59884929-C-G

112836147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59884929-C-T

112836228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59884994-C-T

112836324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59885090-T-G

112836372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59885138-T-C

112836476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59885232-G-T

http://identifiers.org/hco/9/GRCh38#112836516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#59885273-C-A

112836516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59885273-C-T

112836551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59885306-A-G

112836721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59885403-C-T

112837016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59885623-C-T

112837022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59885629-T-C

112837177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59885758-G-A

112838280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59886208-A-G

112838285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59886213-A-T

112838338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59886256-A-G

112838371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59886288-C-T

112838380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59886297-G-T

112838450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59886364-G-A

http://identifiers.org/hco/9/GRCh38#112838467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59886381-A-C

112838492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 59886401-G-A

112838535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 59886444-C-G

112838845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59886708-A-G

112838934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59886791-C-T

112838935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59886792-A-G

112841236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59887990-C-T

112841443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59888206-G-A

112841577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59888331-G-C

112841597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59888351-A-G

112841602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59888356-C-T

112841672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59888383-T-C

112841745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59888453-G-A

112841745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59888453-G-C

112847025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59889060-A-T

http://identifiers.org/hco/9/GRCh38#112847578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59889422-A-C

http://identifiers.org/hco/9/GRCh38#112847741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59889603-A-C

112847741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59889603-A-G

http://identifiers.org/hco/9/GRCh38#112847915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59889718-A-C

112848219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59889890-G-A

112848219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59889890-G-T

112848630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59890251-G-A

112848727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59890348-A-G

112848754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59890364-G-T

http://identifiers.org/hco/9/GRCh38#112848971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59890586-C-A

112849294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59890905-C-G

112849344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59890957-T-C

112849519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59891106-A-G

112849604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59891168-T-G

112849708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59891233-A-G

112850068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59891557-A-T

112850249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59891723-G-T

http://identifiers.org/hco/9/GRCh38#112850718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59892379-C-A

112850718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59892379-C-T

http://identifiers.org/hco/9/GRCh38#112850726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59892387-C-A

112850762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59892406-A-G

112850960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59892563-C-T

112863642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59894060-C-T

112863835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59894243-G-A

http://identifiers.org/hco/9/GRCh38#112863892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59894271-A-C

http://identifiers.org/hco/9/GRCh38#112864234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59894514-C-A

112864234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59894514-C-T

112864244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 59894522-C-G

112864244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 59894522-C-T

112866145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59897434-T-C

http://identifiers.org/hco/9/GRCh38#112866537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59897807-C-A

112866537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59897807-C-T

112866552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59897828-A-G

http://identifiers.org/hco/9/GRCh38#112866669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59897983-C-A

112866669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59897983-C-G

112866669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59897983-C-T

112867911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59898066-C-T

http://identifiers.org/hco/9/GRCh38#112867971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59898137-A-C

112867995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59898161-T-C

112868404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59898599-G-A

112868447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59898642-G-A

112868462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59898657-G-A

112868484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59898672-G-A

112868704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59898854-G-C

112868711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59898860-T-C

http://identifiers.org/hco/9/GRCh38#112868776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59898900-C-A

112868776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 59898900-C-G

112868776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 59898900-C-T

112868828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59898952-A-G

112869123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59899221-A-G

112869133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59899231-A-G

112869234-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59899316-T-G

112869245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59899326-C-T

112869283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59899362-G-T

112869319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59899398-G-A

112869319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59899398-G-C

112869319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59899398-G-T

112869329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59899411-A-G

112869329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59899411-A-T

112869350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59899432-G-A

112869350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59899432-G-T

112869380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59899476-T-A

112869380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59899476-T-C

http://identifiers.org/hco/9/GRCh38#112869441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59899538-A-C

112869441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59899538-A-G

112869669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59899743-T-C

112870032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59900068-G-T

http://identifiers.org/hco/9/GRCh38#112870095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59900126-C-A

http://identifiers.org/hco/9/GRCh38#112870328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59900331-C-A

112870328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59900331-C-T

112870394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59900391-C-T

112870406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59900401-G-A

112870406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59900401-G-T

112870713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59900686-G-T

112870718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59900691-G-T

112870756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59900727-C-T

112870761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59900732-T-C

112871283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59901205-G-C

http://identifiers.org/hco/9/GRCh38#112871378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59901298-C-A

112871378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59901298-C-T

112871414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59901330-G-A

112871598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59901501-G-T

http://identifiers.org/hco/9/GRCh38#112871637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59901539-C-A

112871637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59901539-C-G

112871637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59901539-C-T

112871686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59901650-T-A

112871686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59901650-T-C

http://identifiers.org/hco/9/GRCh38#112871801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59901879-C-A

112871801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59901879-C-T

112871915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59901981-A-G

http://identifiers.org/hco/9/GRCh38#112871940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59902005-A-C

112872050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902089-T-G

112872055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902099-C-T

112872226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902224-G-A

112872226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902224-G-T

112872316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902287-C-T

112872361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902327-T-C

112872367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902333-T-C

112872369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902335-G-T

112872416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902380-G-A

112872416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902380-G-T

112872479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902439-G-A

112872479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902439-G-T

http://identifiers.org/hco/9/GRCh38#112872487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59902447-C-A

112872487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902447-C-T

112872501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902460-G-A

112872501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902460-G-T

http://identifiers.org/hco/9/GRCh38#112872600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59902565-C-A

112872600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902565-C-T

http://identifiers.org/hco/9/GRCh38#112872603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59902568-C-A

112872603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902568-C-T

http://identifiers.org/hco/9/GRCh38#112872641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59902594-C-A

112872803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902717-C-G

112872803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902717-C-T

112872861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902778-G-T

112872917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902831-T-A

112872970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902868-G-A

112872970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902868-G-T

http://identifiers.org/hco/9/GRCh38#112872973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59902871-A-C

112872974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902872-T-C

http://identifiers.org/hco/9/GRCh38#112873044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59902938-C-A

112873044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902938-C-T

112873068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59902962-G-T

112873191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59903072-T-C

112873405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59903271-C-G

112873883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59903721-A-G

112874008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59903817-G-A

112874008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59903817-G-T

112874028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59903837-A-G

112874073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59903878-A-G

http://identifiers.org/hco/9/GRCh38#112874080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59903885-C-A

112874105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59903905-A-G

112874109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59903909-G-T

112874188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59903939-T-C

112874320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59904084-G-A

112874320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59904084-G-T

112874322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59904086-G-A

112874322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59904086-G-T

112874442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59904202-G-A

112874442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59904202-G-T

http://identifiers.org/hco/9/GRCh38#112875072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59904820-C-A

112875090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59904837-G-C

http://identifiers.org/hco/9/GRCh38#112875115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59904860-C-A

112875115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59904860-C-G

112875165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 59904909-A-G

112875165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 59904909-A-T

http://identifiers.org/hco/9/GRCh38#112875180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59904919-C-A

112875207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59904945-C-T

112875235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59904961-G-A

112875267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59904988-G-A

112875267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59904988-G-T

112879037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59905520-C-G

112879037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59905520-C-T

112879071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59905551-C-T

112879216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59905939-T-C

112879217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59905940-G-A

112879217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59905940-G-T

http://identifiers.org/hco/9/GRCh38#112879226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59905964-C-A

112879226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59905964-C-G

http://identifiers.org/hco/9/GRCh38#112879391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#59906130-C-A

112879391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59906130-C-T

112879411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59906148-A-G

112879417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59906154-G-A

112879433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59906164-A-G

112879437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59906168-G-A

112879437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59906168-G-T

112885096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 59909374-G-T

http://identifiers.org/hco/9/GRCh38#112885266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23685
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#59909524-C-A