88067934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: missense variant
orthologous variants: 71239117-A-T

88068005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71239046-T-C

http://identifiers.org/hco/2/GRCh38#88068058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71238895-A-C

http://identifiers.org/hco/2/GRCh38#88068083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71238844-C-A

88068085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71238842-G-A

88068116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71238746-T-A

88068451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71238352-T-C

88068570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71238202-T-G

88068606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71238166-G-C

88068606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71238166-G-T

88068648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71238132-C-T

88068651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71238129-A-T

88068838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71237580-T-C

88069052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71237419-G-A

88069170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71237285-G-A

88069178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71237277-G-T

88069184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71237273-C-G

88069253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71237197-G-A

88069253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71237197-G-C

88069258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71237192-G-A

88069260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71237184-G-C

88069283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71237161-G-A

88069283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71237161-G-T

88069761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71236645-G-A

88074504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71232668-G-T

88074530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71232654-G-A

88074602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71232576-G-T

http://identifiers.org/hco/2/GRCh38#88074742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71232369-A-C

88074774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71232340-G-A

88074852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71232260-G-A

88074903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71232203-G-A

88075037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71232069-A-G

88075038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71232068-G-A

88075046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71232060-C-T

88076032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71226619-T-G

88077230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71225949-T-C

88079275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71221266-C-G

88079469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71221077-T-C

88079476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71221070-A-G

88079539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71221009-G-A

88080285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71218838-T-G

88080353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71218760-G-A

88080396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71218729-T-C

88080451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71218674-A-G

88080649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71218537-G-A

88080803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71218388-G-A

88080869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71218322-A-G

http://identifiers.org/hco/2/GRCh38#88084407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71216617-A-C

88084504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71216520-G-A

88084547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71216485-G-A

http://identifiers.org/hco/2/GRCh38#88084559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71216473-A-C

88084568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71216464-A-G

88084596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71216436-G-T

88084614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71216427-A-T

88087839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71215773-T-G

88087866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71215739-G-A

88087866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71215739-G-T

http://identifiers.org/hco/2/GRCh38#88087875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71215730-A-C

88087875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71215730-A-T

88088024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71215581-G-A

http://identifiers.org/hco/2/GRCh38#88088082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71215512-C-A

88088083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 71215511-C-T

88088104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71215490-T-G

http://identifiers.org/hco/2/GRCh38#88088125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71215469-C-A

88088125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71215469-C-G

88088125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71215469-C-T

88088188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71215416-G-A

88088188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71215416-G-C

88088188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71215416-G-T

http://identifiers.org/hco/2/GRCh38#88088190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71215414-C-A

http://identifiers.org/hco/2/GRCh38#88088193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71215411-C-A

88088193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71215411-C-T

http://identifiers.org/hco/2/GRCh38#88088194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71215410-C-A

88088297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71215309-C-T

88088470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71215138-G-C

http://identifiers.org/hco/2/GRCh38#88088503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71215107-C-A

88088503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71215107-C-T

88090708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71214874-C-T

http://identifiers.org/hco/2/GRCh38#88090888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71214653-C-A

88090892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71214649-A-G

http://identifiers.org/hco/2/GRCh38#88090893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71214648-C-A

88090893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71214648-C-T

http://identifiers.org/hco/2/GRCh38#88090902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71214639-C-A

88090933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71214552-T-C

http://identifiers.org/hco/2/GRCh38#88091002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71214479-C-A

88091002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71214479-C-T

http://identifiers.org/hco/2/GRCh38#88091021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71214460-A-C

88091060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, missense_variant
orthologous variants: 71214421-G-A

88091063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, missense_variant
orthologous variants: 71214418-G-A

http://identifiers.org/hco/2/GRCh38#88091219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71214295-C-A

88091219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71214295-C-T

http://identifiers.org/hco/2/GRCh38#88091243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71214271-C-A

88091243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71214271-C-G

88091243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71214271-C-T

http://identifiers.org/hco/2/GRCh38#88091247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71214267-C-A

88091333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71214188-T-C

88091379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71214151-G-T

88091531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71213973-A-G

88092026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71213847-G-C

88092026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71213847-G-T

88092029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71213844-C-G

88092144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71213750-C-T

88092167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71213745-C-T

88092302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71213611-G-A

88092450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71213583-T-A

88092546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71213489-A-G

http://identifiers.org/hco/2/GRCh38#88092601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71213434-A-C

88092740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71213295-G-A

http://identifiers.org/hco/2/GRCh38#88092881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71213165-A-C

88092882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71213164-C-T

88093332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71212527-T-C

88093332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71212527-T-G

88093342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71212517-C-T

http://identifiers.org/hco/2/GRCh38#88093347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71212512-C-A

88093383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71212476-G-T

88093563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 71212317-A-G

88093564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71212316-G-A

88093564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71212316-G-T

http://identifiers.org/hco/2/GRCh38#88093573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71212307-A-C

88093578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71212302-C-T

http://identifiers.org/hco/2/GRCh38#88093665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71212218-C-A

88093665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71212218-C-G

88093665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71212218-C-T

http://identifiers.org/hco/2/GRCh38#88093675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71212211-C-A

88093675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71212211-C-T

88093917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71211982-A-G

88094020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71211891-C-T

88094694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71204959-G-A

88094918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71204707-C-G

88095377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71203711-G-A

88095486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71203606-T-C

88095827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71203236-A-G

88095895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71203170-T-C

88095936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71203128-C-G

88095936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71203128-C-T

88096027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71203051-T-C

88096204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71202871-T-C

88096283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71202804-A-G

88096284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71202803-A-G

88096345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71202745-G-C

88096389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71202677-G-A

88096468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71202618-A-G

88096468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71202618-A-T

88096482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71202603-G-A

88096482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71202603-G-T

88096509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71202574-A-T

88096519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71202564-A-G

88096552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71202542-T-C

88096659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, missense_variant
orthologous variants: 71202439-T-G

88096811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71202290-T-C

88096829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71202273-G-A

88096829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71202273-G-C

88096829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71202273-G-T

http://identifiers.org/hco/2/GRCh38#88096841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71202261-C-A

88096841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71202261-C-T

88096844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71202258-G-A

88096844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71202258-G-C

88096844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71202258-G-T

88096931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71202216-G-T

88096933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71202214-G-A

88097391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71201879-C-T

88097392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71201878-C-T

88097404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71201866-G-A

88097425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71201845-G-C

88097435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71201835-G-A

88097612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71200486-T-C

88097620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71200478-G-A

88097620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71200478-G-T

88097879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71200225-G-A

88097879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71200225-G-C

88097944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71200153-G-A

88098351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71199859-C-T

88102914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71198262-G-A

88102914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71198262-G-C

88102914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71198262-G-T

88102947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71198230-A-G

http://identifiers.org/hco/2/GRCh38#88102961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71198216-C-A

88102961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71198216-C-T

88103051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 71198009-T-C

88103097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, missense_variant
orthologous variants: 71197963-A-G

http://identifiers.org/hco/2/GRCh38#88103145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71197915-C-A

88103167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71197895-T-C

88103191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71197871-G-A

88103191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71197871-G-T

http://identifiers.org/hco/2/GRCh38#88103226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71197842-C-A

88103226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71197842-C-G

88103226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71197842-C-T

88103227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71197841-G-A

88103227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71197841-G-C

88103227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71197841-G-T

88103253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71197824-G-A

88103253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71197824-G-C

88103253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71197824-G-T

88103416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71197673-G-C

http://identifiers.org/hco/2/GRCh38#88103443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71197645-C-A

88103443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71197645-C-T

88103733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71197392-G-C

88106030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71196677-G-T

88106049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71196658-T-C

88106050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71196657-A-G

88106105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71196606-C-T

http://identifiers.org/hco/2/GRCh38#88106206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71196504-C-A

http://identifiers.org/hco/2/GRCh38#88106261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71196465-C-A

88106261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71196465-C-T

88106262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71196464-G-A

88106262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71196464-G-C

88106266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71196460-G-A

88106529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71196200-G-T

88106555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71196174-A-G

http://identifiers.org/hco/2/GRCh38#88106595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71196138-C-A

88106595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71196138-C-T

88106687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71196025-G-A

88108423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, missense_variant
orthologous variants: 71193826-G-A

88108455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 71193794-G-A

88108471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, missense_variant
orthologous variants: 71193778-A-G

88108592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71193655-A-G

88108592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71193655-A-T

88108596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71193651-G-C

88108596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71193651-G-T

http://identifiers.org/hco/2/GRCh38#88108617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71193630-C-A

88108624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71193622-A-G

http://identifiers.org/hco/2/GRCh38#88108627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71193619-A-C

http://identifiers.org/hco/2/GRCh38#88108632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71193607-C-A

http://identifiers.org/hco/2/GRCh38#88108641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71193598-C-A

88108641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71193598-C-G

88108641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71193598-C-T

88108644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71193595-A-G

88108644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71193595-A-T

http://identifiers.org/hco/2/GRCh38#88108652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71193587-A-C

88109807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71193445-G-A

88110010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71193212-A-G

88110030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71193192-C-T

88110183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71193043-T-C

88110275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71192967-A-G

88110286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71192956-G-A

88110286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron variant
orthologous variants: 71192956-G-T

88110436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, missense_variant
orthologous variants: 71192809-T-A

88110436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, missense_variant
orthologous variants: 71192809-T-C

88110479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 71192766-G-A

88110479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: intron_variant, missense_variant
orthologous variants: 71192766-G-T

88110533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192712-G-A

88110540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192705-T-C

http://identifiers.org/hco/2/GRCh38#88110662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71192662-C-A

88110662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192662-C-G

88110662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192662-C-T

88110725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192609-C-T

http://identifiers.org/hco/2/GRCh38#88110734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71192600-A-C

88110734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192600-A-G

88110751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192586-G-T

http://identifiers.org/hco/2/GRCh38#88110754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71192583-C-A

88110754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192583-C-T

88110755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192582-T-A

88110755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192582-T-C

http://identifiers.org/hco/2/GRCh38#88110825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71192512-A-C

http://identifiers.org/hco/2/GRCh38#88110841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71192496-C-A

88110841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192496-C-T

88110848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192489-A-G

88110865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192472-G-T

88110869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192468-A-G

88110876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192461-G-T

88110897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192449-G-A

88110897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192449-G-T

88110903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192443-G-A

88110903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192443-G-T

88110913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192433-G-T

88110954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192406-G-T

88110955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192405-G-A

88110955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192405-G-T

88111003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192357-G-A

88111003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192357-G-C

88111113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192262-G-A

88111113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192262-G-T

http://identifiers.org/hco/2/GRCh38#88111221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71192198-A-C

88111221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192198-A-G

88111221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192198-A-T

88111245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71192174-T-C

88111754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71191766-A-G

88111804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71191724-T-C

88111804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71191724-T-G

http://identifiers.org/hco/2/GRCh38#88111815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71191713-C-A

88111815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71191713-C-G

88111990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71191532-G-C

88112031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71191494-A-G

88112032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71191493-T-A

88112032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71191493-T-C

88112107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 71191417-A-G

88112107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20986
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 71191417-A-T