125063314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37166701-G-A

125063314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37166701-G-T

125063334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37166685-C-G

125063334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37166685-C-T

125063340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37166679-A-G

125063340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37166679-A-T

125063352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_donor_variant
orthologous variants: 37166667-G-A

125063352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_donor_variant
orthologous variants: 37166667-G-T

http://identifiers.org/hco/11/GRCh38#125063356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37166663-C-A

125063356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37166663-C-G

125063356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37166663-C-T

125063386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37166633-C-G

125063523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37166516-G-A

125063523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37166516-G-T

125063535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37166510-T-G

125063770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37166280-C-G

125064050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37165996-T-G

125064052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37165994-G-C

http://identifiers.org/hco/11/GRCh38#125064166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37165874-A-C

125064578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37165689-G-A

http://identifiers.org/hco/11/GRCh38#125064700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37165591-C-A

125064950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37165380-A-G

http://identifiers.org/hco/11/GRCh38#125065072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37165299-A-C

http://identifiers.org/hco/11/GRCh38#125065103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37165268-C-A

125065150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37165225-G-A

125065175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37165201-G-A

125065175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37165201-G-C

125065299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37165074-A-G

http://identifiers.org/hco/11/GRCh38#125065343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37165021-C-A

125065343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37165021-C-G

125065343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37165021-C-T

125065353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37165011-G-C

125067406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37162672-G-T

125067465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37162619-A-G

http://identifiers.org/hco/11/GRCh38#125067521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37162563-A-C

125067529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37162555-A-G

125067561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37162522-A-G

125067749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37162340-A-T

125068078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37162043-C-T

http://identifiers.org/hco/11/GRCh38#125068213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37161918-C-A

125068251-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37161880-A-T

125068579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37161513-A-G

125068579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37161513-A-T

125068651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37161384-A-G

125068741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37161306-A-G

125068748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37161299-A-T

125068773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37161285-A-G

125068773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37161285-A-T

125068900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37161161-T-A

125069037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37161052-A-G

125069068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37161032-G-A

125069075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37161025-G-A

125069206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37160883-A-T

125069740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37160073-G-A

125069799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37160039-T-C

125069970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37159911-G-A

125070146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37159733-G-A

125070171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37159709-T-C

125070374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37159556-C-T

125070713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37159201-T-A

125070920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37158852-G-A

125070957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37158818-T-C

http://identifiers.org/hco/11/GRCh38#125070972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37158806-A-C

125071046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37158735-A-G

125071112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37158340-A-G

125071183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37158268-A-G

125071246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37158162-C-T

125071705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37158047-C-T

125071796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37157944-C-T

125071863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37157871-G-C

125071988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37157748-G-A

125072195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37157497-G-A

125072195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37157497-G-C

125072459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37157239-G-A

125072645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37157087-T-G

125073174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37156622-A-G

125073222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37156585-C-T

125073224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37156583-G-A

125073246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37156560-C-T

125073476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37156383-G-C

125073824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37156080-C-T

125073900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37156044-G-A

125073910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37156041-C-T

125074331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37155611-G-A

125074554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37155387-A-G

http://identifiers.org/hco/11/GRCh38#125074810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37155115-C-A

125074810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37155115-C-T

http://identifiers.org/hco/11/GRCh38#125075237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37154789-C-A

125075318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37154722-T-C

125075318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37154722-T-G

125075364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37154676-A-G

125075664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37154356-A-G

125075903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37154120-T-C

125076090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37153838-C-T

125076173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37153758-G-A

125076288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37153649-T-A

http://identifiers.org/hco/11/GRCh38#125076615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37153377-C-A

125076615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37153377-C-T

125076641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37153327-A-T

125076652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37153316-C-G

125076652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37153316-C-T

125076711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37153294-G-A

125076711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37153294-G-C

125076926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37153044-T-C

125076926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37153044-T-G

125077037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37152911-C-T

http://identifiers.org/hco/11/GRCh38#125077083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37152865-C-A

http://identifiers.org/hco/11/GRCh38#125077114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37152847-C-A

125077114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37152847-C-T

125077150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37152810-T-A

125077150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37152810-T-C

125077150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37152810-T-G

125077180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37152781-T-C

125077180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37152781-T-G

http://identifiers.org/hco/11/GRCh38#125077215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37152690-C-A

125077215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37152690-C-T

125077561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37152354-G-A

125077636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37152243-T-C

125077791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37152103-T-A

125077791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37152103-T-C

125077793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37152101-T-C

125077882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37152008-A-G

125077936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37151954-G-A

125077953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37151937-G-T

125078209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37151724-G-A

125078309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37151613-A-G

125078395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37151551-A-G

125078599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37151484-G-T

125078705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37151427-C-T

125078786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37151345-T-C

125078960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37151193-G-A

125078960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37151193-G-C

125078960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37151193-G-T

125079013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37151139-G-A

125079013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37151139-G-T

125079026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37151126-C-G

125079057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37151101-G-T

125079061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37151097-T-C

125079116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37151044-G-A

125079152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37151008-T-G

125079173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37150987-G-A

125079185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37150975-T-C

125079323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37150828-G-T

125079382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37150784-T-C

125079382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37150784-T-G

125079532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37150630-G-A

125079532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37150630-G-T

http://identifiers.org/hco/11/GRCh38#125079548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37150614-A-C

125079548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37150614-A-G

125079574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37150588-G-A

125079574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37150588-G-T

125079577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37150584-G-A

125079577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37150584-G-T

125079587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37150574-G-A

125079619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37150542-G-A

125079619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37150542-G-C

125079619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37150542-G-T

http://identifiers.org/hco/11/GRCh38#125079645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37150538-C-A

125079645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37150538-C-T

125079785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37150400-T-A

125079785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37150400-T-C

125079785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37150400-T-G

125079797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37150378-G-A

125079797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37150378-G-T

125080214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37150058-G-C

http://identifiers.org/hco/11/GRCh38#125080501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37149936-C-A

125080501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37149936-C-T

125080515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37149922-A-G

http://identifiers.org/hco/11/GRCh38#125080545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37149892-C-A

125080545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37149892-C-T

http://identifiers.org/hco/11/GRCh38#125080546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37149891-A-C

http://identifiers.org/hco/11/GRCh38#125080551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37149866-C-A

125080568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37149774-T-C

125080750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37149540-G-A

125080750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37149540-G-T

125080880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37149411-G-T

125081072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37149280-G-T

http://identifiers.org/hco/11/GRCh38#125081224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37149209-C-A

125081275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37149177-G-T

125081302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37149160-G-A

125081331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37149136-G-C

125081331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37149136-G-T

http://identifiers.org/hco/11/GRCh38#125081347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37149120-A-C

125081347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37149120-A-G

125081347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37149120-A-T

125081385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37149107-T-A

125081385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37149107-T-C

125081385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37149107-T-G

125081473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37149018-T-C

125081510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148986-G-A

125081510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148986-G-C

125081515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148981-G-A

125081515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148981-G-T

125081516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148980-A-G

http://identifiers.org/hco/11/GRCh38#125081536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37148962-C-A

125081536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148962-C-T

http://identifiers.org/hco/11/GRCh38#125081573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37148924-A-C

125081573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148924-A-G

125081573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148924-A-T

http://identifiers.org/hco/11/GRCh38#125081574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37148923-C-A

125081574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148923-C-T

http://identifiers.org/hco/11/GRCh38#125081576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37148921-C-A

125081576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148921-C-T

125081627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148872-G-A

125081627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148872-G-C

125081627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148872-G-T

125081662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148839-G-A

125081662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148839-G-C

125081662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148839-G-T

125081673-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148827-T-A

125081674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148826-C-T

125081680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148820-C-T

125081792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37148708-T-C

125081972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148531-G-A

125081972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148531-G-C

125081972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148531-G-T

125081976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148527-G-A

125081976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148527-G-T

125081980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148523-G-A

125081980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148523-G-T

125082100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148408-T-C

http://identifiers.org/hco/11/GRCh38#125082184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37148325-C-A

125082220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148288-T-A

125082301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37148206-C-G

125082343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148164-A-G

125082393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148108-G-T

http://identifiers.org/hco/11/GRCh38#125082428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37148079-C-A

125082554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37148032-T-A

http://identifiers.org/hco/11/GRCh38#125082749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37147886-C-A

125082779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37147868-G-A

125082995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37147651-G-A

125082995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37147651-G-T

125083045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37147601-T-A

125083045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37147601-T-C

125083120-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37147531-T-A

125083120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37147531-T-C

125083127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37147524-T-C

http://identifiers.org/hco/11/GRCh38#125083180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#37147457-C-A

125083180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 37147457-C-T

125083238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 37147395-G-A

125083287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 37147348-G-C

125083300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 37147335-G-A

125083300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 37147335-G-T

125083379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37147275-T-C

http://identifiers.org/hco/11/GRCh38#125083401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37147252-C-A

125083401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37147252-C-T

http://identifiers.org/hco/11/GRCh38#125083414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37147239-C-A

125083414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37147239-C-T

http://identifiers.org/hco/11/GRCh38#125083434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37147213-A-C

125083434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37147213-A-G

http://identifiers.org/hco/11/GRCh38#125083492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37147149-C-A

125083492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37147149-C-T

http://identifiers.org/hco/11/GRCh38#125083542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37147102-C-A

125083542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37147102-C-T

125083543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37147101-A-G

125083550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37147094-A-G

125083572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37147074-T-G

125083632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37147017-G-T

125083733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37146926-G-A

125083733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37146926-G-T

http://identifiers.org/hco/11/GRCh38#125083774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37146883-C-A

125083774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37146883-C-T

125083888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37146764-G-A

http://identifiers.org/hco/11/GRCh38#125083914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37146738-C-A

125083914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37146738-C-G

125083914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37146738-C-T

125083971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37146684-G-T

125084156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37146526-G-A

125084212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37146486-C-T

http://identifiers.org/hco/11/GRCh38#125084386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37146318-A-C

125084386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37146318-A-G

125084386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37146318-A-T

125084423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37146280-G-A

125084423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37146280-G-T

125084659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145879-G-A

http://identifiers.org/hco/11/GRCh38#125084709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37145828-A-C

125084709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145828-A-G

125084748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145794-T-C

125084750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145792-G-A

125084918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145643-T-C

http://identifiers.org/hco/11/GRCh38#125085164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37145431-C-A

125085164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145431-C-T

http://identifiers.org/hco/11/GRCh38#125085165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37145430-C-A

125085165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145430-C-T

125085168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145427-G-A

125085168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145427-G-C

125085168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145427-G-T

http://identifiers.org/hco/11/GRCh38#125085225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37145372-C-A

125085225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145372-C-T

http://identifiers.org/hco/11/GRCh38#125085246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37145363-C-A

125085246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145363-C-G

125085246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145363-C-T

http://identifiers.org/hco/11/GRCh38#125085256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37145353-C-A

125085256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145353-C-T

125085263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145346-A-G

125085267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145343-A-G

http://identifiers.org/hco/11/GRCh38#125085269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37145341-C-A

125085269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145341-C-G

125085269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145341-C-T

125085271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145339-T-C

125085271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145339-T-G

http://identifiers.org/hco/11/GRCh38#125085315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37145296-C-A

125085315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145296-C-G

125085315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145296-C-T

125085318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145293-A-G

125085347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37145265-T-A

http://identifiers.org/hco/11/GRCh38#125085376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37145233-C-A

125085654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37144934-G-A

125085848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37144764-T-C

125085848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37144764-T-G

125085867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37144742-G-C

125085867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37144742-G-T

125085940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37144683-C-G

125085940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37144683-C-T

125086187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37144420-C-T

125086330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37144276-T-C

125086330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37144276-T-G

125086343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37144264-T-C

125086414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37144186-G-T

125086426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37144174-A-G

http://identifiers.org/hco/11/GRCh38#125086497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37144136-C-A

125086497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37144136-C-T

125086553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37144082-A-G

125086621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37144021-A-G

125086659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143983-A-G

125086676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143973-T-A

125086676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143973-T-G

125086677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143972-G-A

125086677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143972-G-T

125086795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143864-T-C

125086813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143838-G-T

125086939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143723-A-T

125086971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143693-G-A

125086971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143693-G-T

125086978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143686-A-G

125086999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143671-A-G

http://identifiers.org/hco/11/GRCh38#125087014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37143656-C-A

http://identifiers.org/hco/11/GRCh38#125087019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37143651-C-A

125087019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143651-C-T

125087040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143630-A-G

125087080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143595-T-A

125087080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143595-T-C

125087081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143594-G-A

125087288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143384-T-A

125087288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143384-T-C

125087288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143384-T-G

http://identifiers.org/hco/11/GRCh38#125087300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37143372-C-A

http://identifiers.org/hco/11/GRCh38#125087326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37143349-C-A

125087377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143313-G-T

125087452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143233-T-C

125087540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143168-G-T

125087560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143148-T-A

125087560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143148-T-C

125087560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143148-T-G

125087613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143092-T-C

125087614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37143091-G-A

http://identifiers.org/hco/11/GRCh38#125088077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37142992-C-A

125088077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37142992-C-T

125088104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37142965-C-T

125088194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142882-G-A

125088194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142882-G-T

125088279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142802-G-A

125088279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142802-G-T

http://identifiers.org/hco/11/GRCh38#125088318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37142755-C-A

125088342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142731-A-G

125088366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142707-A-G

125088381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142692-G-A

125088381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142692-G-T

125088430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142663-G-A

125088430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142663-G-C

125088478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142638-G-A

125088478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142638-G-C

125088478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142638-G-T

125088491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142625-G-A

125088491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142625-G-C

125088491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142625-G-T

http://identifiers.org/hco/11/GRCh38#125088572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37142544-C-A

125088572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142544-C-T

http://identifiers.org/hco/11/GRCh38#125088573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37142543-C-A

125088573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142543-C-T

http://identifiers.org/hco/11/GRCh38#125088594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37142518-A-C

125088594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142518-A-G

125088600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142512-G-A

125088600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142512-G-C

125088600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142512-G-T

http://identifiers.org/hco/11/GRCh38#125088637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37142460-C-A

http://identifiers.org/hco/11/GRCh38#125088650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37142444-C-A

125088650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142444-C-T

http://identifiers.org/hco/11/GRCh38#125088688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37142404-C-A

125088688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142404-C-T

125088690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142402-G-A

125088690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142402-G-T

125088723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142369-A-T

http://identifiers.org/hco/11/GRCh38#125088765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37142329-C-A

125088771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142317-C-G

125088771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142317-C-T

http://identifiers.org/hco/11/GRCh38#125088855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37142236-C-A

125088855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142236-C-T

125088857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142234-G-A

125088857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142234-G-T

125088971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142143-T-A

125088971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142143-T-G

125088977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142137-G-T

125088989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142125-A-G

125089076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142047-G-A

125089076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37142047-G-T

http://identifiers.org/hco/11/GRCh38#125089257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37141862-C-A

125089257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37141862-C-T

125089285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37141832-T-G

125089299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37141818-G-A

125089299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37141818-G-T