166666130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166470808-G-T

166666394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166470588-T-C

166666531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166470449-C-T

166666532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166470448-G-A

166668564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166470342-C-T

166668827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166470092-C-T

166668902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166470024-A-G

166669057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166469904-T-C

166669078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166469883-G-A

166669078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166469883-G-T

166669126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166469835-T-C

http://identifiers.org/hco/1/GRCh38#166669131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166469830-C-A

166669221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166469740-G-T

166669222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 166469739-A-G

166669224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166469738-T-C

http://identifiers.org/hco/1/GRCh38#166669237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166469725-C-A

166669237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166469725-C-T

166669239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166469723-T-C

http://identifiers.org/hco/1/GRCh38#166669319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166469658-A-C

166669340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166469653-T-C

http://identifiers.org/hco/1/GRCh38#166669346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166469647-A-C

166669346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166469647-A-G

166669346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166469647-A-T

166669360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166469633-T-C

166669455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166469538-A-G

http://identifiers.org/hco/1/GRCh38#166669543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166469446-C-A

166669543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166469446-C-T

166669553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166469436-A-G

166669647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166469371-A-G

166669689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166469333-A-G

166669740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166469282-G-A

http://identifiers.org/hco/1/GRCh38#166669756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166469266-C-A

166669756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166469266-C-T

166669763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166469259-G-A

166669807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166469215-G-A

166669807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166469215-G-C

166669876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166469146-A-G

166669876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166469146-A-T

166669894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166469128-A-T

166669909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166469111-G-A

166669947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166469079-T-C

166669951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166469075-G-T

166670077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468956-T-C

166670101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468932-C-T

166670147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468887-T-C

166670205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468842-C-T

166670233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468818-G-T

166670239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468812-G-A

166670245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468806-A-G

166670321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468643-T-C

http://identifiers.org/hco/1/GRCh38#166670327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166468637-C-A

166670327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468637-C-G

166670327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468637-C-T

166670337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468629-G-C

166670477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468512-C-G

166670477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468512-C-T

166670492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468497-T-A

166670506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468483-T-C

166670525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468466-T-A

166670548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468446-C-T

166670954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468337-T-C

166671186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468225-T-C

166671232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468181-A-G

166671240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468173-T-G

166671295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468125-T-G

166671375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468049-G-T

166671412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166468013-G-A

166671532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166467869-T-A

166671547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166467854-A-G

166671572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166467838-T-G

166671595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166467817-C-T

http://identifiers.org/hco/1/GRCh38#166671598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166467816-C-A

166671598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166467816-C-T

166671611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166467803-G-A

166671611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166467803-G-C

166671639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166467775-A-G

166671642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166467772-A-G

166671646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166467768-A-G

http://identifiers.org/hco/1/GRCh38#166671655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166467759-A-C

166671658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166467756-C-T

166671733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166467683-A-G

166671733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166467683-A-T

http://identifiers.org/hco/1/GRCh38#166671758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166467658-C-A

http://identifiers.org/hco/1/GRCh38#166671761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166467655-C-A

166671803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166467613-G-A

166671803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166467613-G-T

166671827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166467589-G-T

http://identifiers.org/hco/1/GRCh38#166671839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166467577-C-A

166671840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166467576-A-G

166671842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166467574-G-T

166671876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166467540-T-C

166671884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166467531-G-T

166671922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166467501-G-T

166671927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166467496-G-T

166672213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166467229-A-G

166672218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166467224-C-T

166672239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166467200-T-C

166672351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166467101-G-C

166672449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166467015-C-T

http://identifiers.org/hco/1/GRCh38#166672472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166466999-A-C

http://identifiers.org/hco/1/GRCh38#166672549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166466956-A-C

166672549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166466956-A-T

166672566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166466942-A-G

166672679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166466802-C-T

166673002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166466433-T-A

166673067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166318083-C-G

166673073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166318078-G-A

166673262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166466108-G-A

166673262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166466108-G-T

166673266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166466104-G-T

166673269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166466101-G-A

166673269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166466101-G-T

166673279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166466091-A-G

166673308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166466062-A-G

166673309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166466061-G-A

166673321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166466041-A-G

http://identifiers.org/hco/1/GRCh38#166673399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166465949-C-A

166673625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166465727-A-G

166673666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166465678-T-C

166673681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166465664-G-C

166673683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166465662-A-G

166673684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166465661-A-G

166673803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166465382-G-A

166673803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166465382-G-T

166673874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166465284-A-G

166673892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166465267-C-T

166673925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166465233-C-T

166673954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166465214-G-C

166673957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166465211-A-G

166673983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166465188-C-T

166674090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166465097-A-G

http://identifiers.org/hco/1/GRCh38#166674108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166465079-C-A

166674166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166465022-G-A

166674243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166464943-T-A

166674244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166464942-C-T

166674309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166464832-C-T

166674368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166464697-C-T

166674371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166464694-C-G

http://identifiers.org/hco/1/GRCh38#166674412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166464510-A-C

http://identifiers.org/hco/1/GRCh38#166674452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166464409-C-A

166674585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166464277-A-G

http://identifiers.org/hco/1/GRCh38#166674615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166464234-C-A

166674702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166464180-T-C

166674828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166462981-G-A

166674960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166462875-T-C

166674988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166462847-T-C

166675236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166462614-C-G

http://identifiers.org/hco/1/GRCh38#166675237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166462613-C-A

166675307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166462543-A-G

http://identifiers.org/hco/1/GRCh38#166675481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166462373-C-A

166675481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166462373-C-T

166675520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166462334-A-G

166675521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166462333-G-A

166675521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166462333-G-T

166675532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166462322-G-T

http://identifiers.org/hco/1/GRCh38#166675636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166462229-A-C

166675636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166462229-A-G

166675637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166462228-T-C

166676827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166461988-T-C

166676925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166461953-G-T

http://identifiers.org/hco/1/GRCh38#166677462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166461303-C-A

166677462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166461303-C-G

166677462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166461303-C-T

166677466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166461299-T-G

166677486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166461279-G-A

166677486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166461279-G-T

166677568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166461189-A-G

http://identifiers.org/hco/1/GRCh38#166677668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166461090-A-C

166677668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166461090-A-T

166677679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166461079-T-C

166677709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166461049-C-G

166677709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166461049-C-T

166677794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460963-G-T

166677800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460957-T-G

http://identifiers.org/hco/1/GRCh38#166677916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166460849-C-A

166677932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460831-A-G

166677945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460815-T-G

166677990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460784-T-C

http://identifiers.org/hco/1/GRCh38#166678055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166460702-A-C

166678055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460702-A-G

166678069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460688-A-T

http://identifiers.org/hco/1/GRCh38#166678120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166460641-C-A

166678129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460632-C-T

166678169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460590-A-G

166678229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460532-A-G

166678252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460508-G-A

166678253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460507-G-A

http://identifiers.org/hco/1/GRCh38#166678266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166460494-C-A

166678266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460494-C-T

166678286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460472-G-C

166678287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460471-A-T

166678309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460446-T-C

166678359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460397-G-T

166678366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460390-A-G

166678386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460374-C-G

166678432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460328-C-T

166678454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 166460302-T-G

166678483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166460273-A-G

166678490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166460266-C-T

http://identifiers.org/hco/1/GRCh38#166678500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166460256-C-A

166678500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166460256-C-T

166678506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166460250-G-C

166678537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460216-T-A

http://identifiers.org/hco/1/GRCh38#166678554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166460199-A-C

http://identifiers.org/hco/1/GRCh38#166678590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166460163-C-A

166678660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460091-G-T

166678682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460086-G-A

166678690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460078-A-T

166678700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460066-T-C

166678738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166460028-G-T

166681274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166312195-C-G

166681561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166311947-C-T

166681656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166311850-T-G

166681907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166311637-G-A

166681907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166311637-G-T

166682183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166311360-G-A

166682183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166311360-G-T

http://identifiers.org/hco/1/GRCh38#166682188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#166311355-C-A

166682188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32211
most severe consequence: non coding transcript exon variant
orthologous variants: 166311355-C-T