102190801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55344408-G-A

http://identifiers.org/hco/3/GRCh38#102190813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55344392-A-C

102191264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55343983-A-G

102191590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55343639-T-C

http://identifiers.org/hco/3/GRCh38#102191622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55343610-C-A

102191811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55343442-A-G

http://identifiers.org/hco/3/GRCh38#102191866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55343379-A-C

102191888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55343355-G-A

102191935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55343307-C-T

102191984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55343257-C-T

102191988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55343253-G-A

102192003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55343238-T-C

102192102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55343134-G-T

http://identifiers.org/hco/3/GRCh38#102192214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55343031-C-A

102192214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55343031-C-G

http://identifiers.org/hco/3/GRCh38#102192251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55342994-C-A

http://identifiers.org/hco/3/GRCh38#102192272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55342981-C-A

102192299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55342957-G-T

102192425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55342839-G-T

102192482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55342737-G-T

102192546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55342683-G-A

102192546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55342683-G-T

102192549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55342680-A-T

102192694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55342541-T-A

102192708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55342527-T-C

102192721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55342514-A-G

102192758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55342477-C-T

102192794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55342441-T-C

102192972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55342075-G-A

102192972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55342075-G-T

102193050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55342001-C-G

102193106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55341955-A-G

102193119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55341942-C-T

102193152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55341909-T-C

102193216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55341850-G-A

102193217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55341849-C-G

102193220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55341846-T-C

102193220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55341846-T-G

102193445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55341775-T-A

102193447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55341773-A-G

102193480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55341737-A-G

102194096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55341351-C-G

102194143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55341308-A-G

102194270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55341169-A-G

102194399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55341039-G-C

102194750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55326342-A-T

102195305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55325632-C-G

102195305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55325632-C-T

102195412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55325543-T-A

102195477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55325447-T-C

102195537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55325391-T-A

http://identifiers.org/hco/3/GRCh38#102195756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55325163-C-A

102197020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55324984-T-C

102197160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55324828-C-T

102197176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55324812-T-A

http://identifiers.org/hco/3/GRCh38#102197209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55324780-A-C

102197209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55324780-A-G

102197209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55324780-A-T

http://identifiers.org/hco/3/GRCh38#102197253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55324684-A-C

102197287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55324611-G-A

102197739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55324186-C-T

102197783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55324142-C-T

102197789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55324069-G-A

102197832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55324026-G-A

102218576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55304597-T-C

102218613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55304563-T-C

102218654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55304522-T-A

102218654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55304522-T-C

102218660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55304516-A-G

102218722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55304435-G-C

102218774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55304380-C-T

102223596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55302215-A-G

102223624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55302183-C-T

102223646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55302175-A-G

102223659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55302159-G-T

102223662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55302156-C-T

102223753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55302062-G-A

102223761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55302054-T-C

102223776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55302039-C-G

102223779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55302036-G-A

102223788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55302028-T-C

102223804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55302012-T-C

102223931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55301896-C-T

102223948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55301880-A-G

102224107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55301730-T-C

102224417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55301410-G-A

102224503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55301321-T-C

102224540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55301285-T-A

102225199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55301194-A-G

102225403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55300994-A-G

102225519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55300880-G-C

102225618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55300787-A-G

102226214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55300518-C-G

102226321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55300416-G-A

102226321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55300416-G-T

102226377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55300365-G-A

http://identifiers.org/hco/3/GRCh38#102226391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55300351-C-A

102226391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55300351-C-T

102226800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55299642-G-A

102226936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55299528-T-C

102226945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55299520-C-T

102227053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55299265-T-G

102227069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55299249-T-G

102227194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55299136-C-T

102227338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55299007-G-A

102227367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55298976-G-T

102227762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55298593-T-C

102228075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55298324-G-A

102228233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55298153-T-G

102228281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55298105-C-T

102228313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55298075-A-T

http://identifiers.org/hco/3/GRCh38#102228462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55297943-A-C

102228572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55297840-G-C

102228627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55297785-A-G

102228627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55297785-A-T

102228672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55297738-C-G

102228690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55297722-C-T

http://identifiers.org/hco/3/GRCh38#102228694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55297718-A-C

102228694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55297718-A-G

http://identifiers.org/hco/3/GRCh38#102229014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55297523-C-A

102229018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55297519-T-A

102229018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55297519-T-C

102229069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55297478-T-A

102229251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55297374-G-A

102229251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55297374-G-T

102229301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55297326-T-A

102229326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55297308-G-A

102229326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55297308-G-T

102229543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55297088-C-T

102229618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55297000-T-C

102229638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55296980-A-G

102229708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55296909-T-C

102229739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55296886-T-A

102229865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55296762-C-T

102230154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55296666-A-G

102230205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55296632-C-T

102230239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55296614-T-A

102230242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55296611-G-A

102230242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55296611-G-T

102230309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55296591-G-A

102230310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55296590-A-G

102230372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55296538-A-G

102230410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55296511-T-C

102230611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55296415-G-A

102230631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55296397-T-A

http://identifiers.org/hco/3/GRCh38#102230888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55296186-A-C

102230888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55296186-A-G

http://identifiers.org/hco/3/GRCh38#102231016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55296049-A-C

102231243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55295862-A-G

102231435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55295670-G-A

102231435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55295670-G-C

102231672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55295436-G-A

102231704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55295415-C-T

102231915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55295144-T-A

102232269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55293757-T-C

102232308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55293717-T-C

102232358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55293674-T-C

102232358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55293674-T-G

102232416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55293611-G-A

http://identifiers.org/hco/3/GRCh38#102232699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55293353-A-C

102232854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55293217-A-T

102232855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55293216-T-C

102232858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55293213-T-C

102232860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55293211-C-T

102232974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55293089-T-G

102233040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55292964-C-G

http://identifiers.org/hco/3/GRCh38#102233066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55292897-A-C

102233223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55292731-T-G

102233471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55292465-A-G

102233566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55292374-T-C

102233631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55292322-T-C

102234184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55291782-C-G

102234310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55291623-A-T

102234366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55291570-T-C

102234380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55291556-G-T

102234584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55291364-T-G

102235119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55290897-G-A

102235166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55290850-T-C

102235392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55290095-A-G

102235510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55289995-C-T

102235755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55289763-T-C

102235865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55289658-G-T

102235897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55289626-A-G

102236233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55289291-A-G

102236233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55289291-A-T

http://identifiers.org/hco/3/GRCh38#102236240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55289284-C-A

102236245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55289280-G-A

102236263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55289263-T-G

102236324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55289161-A-G

102236478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55289007-C-T

http://identifiers.org/hco/3/GRCh38#102236508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55288980-A-C

102237046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55288490-G-A

102237356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55288247-C-T

102237484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55288118-T-A

102237775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55287789-G-A

102237775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55287789-G-T

102237910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55287653-G-T

102237975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55287588-T-C

102237995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55287568-G-A

102238215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55287343-G-A

102238216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55287342-A-G

102238407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55287188-G-A

102238444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55287151-T-C

102238458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55287136-G-T

102239188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55283798-C-T

102239856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55283240-T-G

102240839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55279883-T-C

102241001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55279686-G-A

102241001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55279686-G-T

102241081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55279604-T-C

102241870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278819-G-A

102241898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278793-A-G

102241951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278739-G-A

102241951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278739-G-T

102242015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278672-G-A

102242027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278664-G-T

102243252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278379-G-A

102243252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278379-G-C

102243335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278286-C-G

102243471-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278168-A-T

102243542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278109-T-G

102243618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278032-T-C

102243640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55278010-G-A

102243683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55277967-T-C

102244283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55277115-G-T

102245115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55276618-A-G

102245125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55276608-A-G

102245545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55276388-T-C

http://identifiers.org/hco/3/GRCh38#102245652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55276283-C-A

102245704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55276229-T-C

102245807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55276134-C-T

102246405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55275867-C-G

102246503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55275765-A-T

102246522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55275746-T-C

102246721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55275530-A-T

102246959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55275297-A-G

102247135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55275131-G-A

102247135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55275131-G-T

http://identifiers.org/hco/3/GRCh38#102247173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55275095-C-A

102247299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55274988-G-A

102247299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55274988-G-T

102247337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55274959-C-T

102247371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55274923-G-C

102247899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55274317-T-G

102248300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55273956-T-G

102248635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55273858-T-A

102248635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55273858-T-G

http://identifiers.org/hco/3/GRCh38#102248789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55273730-C-A

102248813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55273704-T-C

102248846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55273660-A-T

102249630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55273347-T-C

http://identifiers.org/hco/3/GRCh38#102250153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55272823-C-A

102250153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55272823-C-T

http://identifiers.org/hco/3/GRCh38#102250155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55272821-A-C

102250155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55272821-A-G

102250269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55272708-A-T

102251105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55271870-C-T

102251143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55271832-G-A

102251160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55271815-T-C

102251255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55271718-T-C

102251544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55271056-T-A

http://identifiers.org/hco/3/GRCh38#102251769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55270848-C-A

102251878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55270737-G-A

102251903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55270707-T-C

102251943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55270672-A-G

102252074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55270545-A-G

102252199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55270418-G-T

102252281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55270336-T-C

102252281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55270336-T-G

102252647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269952-A-G

102252651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269948-A-G

102252658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269941-T-G

102252769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269842-G-A

102252900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269704-G-T

102252916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269688-G-A

102252965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269640-T-A

102252989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269603-T-C

102253037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269502-A-G

102253076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269467-G-C

http://identifiers.org/hco/3/GRCh38#102253088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55269455-A-C

102253122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269421-A-G

102253193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269350-T-C

102253306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269236-C-G

102253306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269236-C-T

102253342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269201-T-C

102253758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269048-T-C

102253850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269013-G-A

102253850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55269013-G-C

102253937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55268948-G-A

102254028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55268855-T-C

102254234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55268656-G-A

102254366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55268547-T-C

102255305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55267793-A-T

102255395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55267709-A-T

102255401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55267703-T-C

102255630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55267405-G-A

102255643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55267392-T-C

102255873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55267165-T-G

http://identifiers.org/hco/3/GRCh38#102255973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55267070-A-C

102256027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55267016-A-G

102256123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55266911-G-A

102256123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55266911-G-T

102256420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55266690-G-T

102256890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55265090-G-A

102256954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55265031-G-T

102257217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264951-G-A

102257282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264875-C-T

102257284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264873-T-A

102257616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264581-A-T

102257850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264351-C-T

102257853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264348-T-C

102257877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264324-T-C

102257901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264300-T-A

http://identifiers.org/hco/3/GRCh38#102257918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55264283-A-C

102257931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264269-T-A

102257964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264247-C-T

102258127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264093-C-T

102258186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55264034-T-C

102258351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55263872-T-A

http://identifiers.org/hco/3/GRCh38#102258432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55263792-A-C

102258967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55263263-A-G

102259184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55263004-T-A

http://identifiers.org/hco/3/GRCh38#102259277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55262927-C-A

102259327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55262888-A-T

102264072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55261995-A-G

102264279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55261805-G-T

102264337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55261747-A-G

102264671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55261200-G-A

102264874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55261017-T-C

http://identifiers.org/hco/3/GRCh38#102264898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55260994-C-A

102264898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55260994-C-T

102265097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55260721-A-T

102265128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55260688-A-G

102265129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55260687-T-C

102265328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55260204-T-C

102269052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55256659-G-T

102269464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55256187-C-T

http://identifiers.org/hco/3/GRCh38#102269799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55255863-A-C

102269835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55255826-A-G

102269926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55255443-G-A

102270074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55255288-G-T

102270557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55254853-G-A

102291690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55254731-T-C

102291704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55254717-T-C

102291766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55254647-A-G

102291778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55254635-T-G

102291854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55254560-G-T

102292043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55254370-C-T

102293002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55253759-A-G

102295445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55242724-A-G

http://identifiers.org/hco/3/GRCh38#102295659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55242529-C-A

http://identifiers.org/hco/3/GRCh38#102295906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55242293-C-A

102295971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55242083-G-C

102295971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55242083-G-T

102296198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55241666-T-C

http://identifiers.org/hco/3/GRCh38#102296411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55241465-A-C

102296411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55241465-A-G

102296464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55241413-A-G

102296525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55241352-C-T

http://identifiers.org/hco/3/GRCh38#102296834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55240673-A-C

102296834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55240673-A-G

http://identifiers.org/hco/3/GRCh38#102297128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55240252-C-A

102297151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55240228-T-C

102297259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55240124-C-T

http://identifiers.org/hco/3/GRCh38#102297373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55239718-A-C

102297399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55239688-A-G

102297400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55239687-A-G

102297855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55239245-G-A

102297968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55239128-A-T

102298143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55238920-T-C

102298221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55238840-G-A

102298221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55238840-G-T

102299007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55238249-T-A

102299324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55238013-A-G

102299568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55237813-A-T

102302055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55237198-T-G

102302116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55237139-G-A

102302116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55237139-G-C

102302158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55237098-G-A

http://identifiers.org/hco/3/GRCh38#102302217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55237032-C-A

102302285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55236950-A-G

102302321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55236918-G-A

102302612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55236644-A-G

102302612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55236644-A-T

102303063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55236277-T-C

102303201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55236126-C-T

http://identifiers.org/hco/3/GRCh38#102303329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55236010-C-A

102303466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55235895-T-C

http://identifiers.org/hco/3/GRCh38#102303503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55235858-C-A

102304030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55229831-A-T

102304119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55229759-G-C

102304314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55229577-C-T

102304516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55229350-A-G

102304689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55229187-T-C

102304921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55228649-A-G

102304921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55228649-A-T

102304964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55228570-G-A

102304997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55228503-C-T

102305472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55228010-G-A

102305488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55227996-A-G

102306720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55225909-A-G

102314665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55225581-A-G

102314973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55225283-A-G

102315225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55225033-T-C

102315982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55223735-G-A

http://identifiers.org/hco/3/GRCh38#102316008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55223709-C-A

http://identifiers.org/hco/3/GRCh38#102316429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55223408-A-C

102317069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55222832-A-G

http://identifiers.org/hco/3/GRCh38#102317177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55222719-C-A

102317177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55222719-C-G

102323214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55221624-A-G

102325380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55217156-G-A

102325755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55216946-G-T

102325783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55216920-T-C

102325784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55216919-G-T

102325939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55216727-C-G

102326234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55216443-G-A

102326234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55216443-G-T

http://identifiers.org/hco/3/GRCh38#102326471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55216082-A-C

102326471-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55216082-A-T

102326536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55215783-A-T

102326543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55215718-C-T

102326703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55215542-G-T

http://identifiers.org/hco/3/GRCh38#102326708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55215536-C-A

102326708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55215536-C-T

102326753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55215493-G-T

102326821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55215428-T-C

102326824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55215425-T-G

102326908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55215344-G-A

http://identifiers.org/hco/3/GRCh38#102326917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55215335-A-C

102327176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55215038-T-C

102327741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55214738-A-G

102327769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55214711-C-T

102327803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55214679-A-G

102332486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55213897-A-T

102332969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55213345-A-G

102333020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55213246-G-C

http://identifiers.org/hco/3/GRCh38#102333121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55213130-C-A

102333503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55212736-C-T

102333602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55212058-T-C

102333960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55211726-G-A

http://identifiers.org/hco/3/GRCh38#102333968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55211718-C-A

102333968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55211718-C-T

102334022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55211654-T-C

102334216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55211511-A-G

102334216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55211511-A-T

102334291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55211444-T-A

102334402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55211376-T-A

102334508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55211287-T-G

102334765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55211080-G-A

102334821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55211044-A-G

102337625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55202734-C-T

http://identifiers.org/hco/3/GRCh38#102337721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55202640-A-C

102338070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55202116-A-G

102338084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55202102-T-G

102338166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55202022-G-C

102338239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55201951-C-T

102338303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55201886-G-A

102338303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55201886-G-T

102338451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55201735-T-C

http://identifiers.org/hco/3/GRCh38#102338486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55201707-A-C

102338493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55201699-A-G

102338520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55201668-T-C

102338564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55201625-C-G

102338564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55201625-C-T

102338603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55201585-A-G

102338711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55201473-G-A

102338796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55201393-C-T

102338813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55201371-T-A

102339275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55200910-A-G

102339290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55200895-A-G

102339353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55200851-G-T

102339505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55200698-C-T

102339589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55200615-T-C

102339734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55200473-A-G

102339804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55200404-G-C

102340034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55200182-C-T

102340051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55200167-G-A

102340079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55200144-A-G

102342466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55198270-G-T

102342502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55198246-C-G

102342586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55198119-G-A

102342609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55198051-T-C

102342613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55198047-T-C

102342745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55197865-T-C

102342806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55197808-T-C

102343114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55197531-C-T

102343197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55197469-C-T

http://identifiers.org/hco/3/GRCh38#102343322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55197355-A-C

102343922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55196686-T-C

102343984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55196624-A-G

102343988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55196619-T-C

102344014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55196593-T-A

102344056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55196552-G-C

102344196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55196400-G-T

102344330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55196277-G-A

102345391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55194841-A-G

102345423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55194719-G-T

102345476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55194668-T-C

102345871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55194325-A-G

102346181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55194227-C-T

102346211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55194203-G-A

http://identifiers.org/hco/3/GRCh38#102346838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55193916-C-A

102347035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55193749-T-C

102347054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55193730-C-T

102347055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55193729-C-T

102347924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55192899-C-T

102347957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55192870-T-A

102348448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55192375-T-G

102348695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55191885-T-G

102349031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55191503-A-T

102349044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55191490-C-T

102349322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55191212-T-A

102349441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55191088-G-A

http://identifiers.org/hco/3/GRCh38#102349544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55190988-C-A

102349614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55190925-C-T

102349615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55190924-A-G

102349662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55190902-C-T

102352402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55182772-T-C

102352402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55182772-T-G

http://identifiers.org/hco/3/GRCh38#102352578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55182599-A-C

102352606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55182569-G-T

102358909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55179810-C-G

102358995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55179729-C-T

102359031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55179693-G-A

102359031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55179693-G-T

102359162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55179564-G-A

102359196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55179535-T-G

102359234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55179497-A-G

102359297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55179430-G-A

102359726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55178986-G-A

http://identifiers.org/hco/3/GRCh38#102359752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55178959-C-A

102359752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55178959-C-G

102359997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55178711-G-A

102360121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55178514-A-G

102360314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55178316-C-G

http://identifiers.org/hco/3/GRCh38#102360404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55178226-C-A

102360956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55177157-G-C

102361879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55176244-T-A

102361912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55176217-C-T

102362053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55176074-A-T

102362210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55175895-G-A

102362221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55175884-T-C

http://identifiers.org/hco/3/GRCh38#102362287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55175828-A-C

102370749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55173929-T-G

102371250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55173441-A-G

102371329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55173373-C-T

102371345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55172495-A-G

102371417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55172424-G-T

102371560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55172322-C-G

102371560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55172322-C-T

102371847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55171968-T-C

102371849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55171966-A-T

102371899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55171935-A-G

102371958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55171881-G-A

102371978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55171861-A-G

102371991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55171848-C-T

102372426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55171439-C-T

http://identifiers.org/hco/3/GRCh38#102372502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55171384-C-A

102376003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55170545-A-G

102376014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55170534-T-A

102376014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55170534-T-C

102376295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55170314-C-G

102376298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55170311-T-G

102377751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55169642-A-G

102377813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55169581-A-G

102377813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55169581-A-T

102377848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55169547-G-A

102377848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55169547-G-T

102377914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55169478-T-C

102377964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55169434-A-G

102378057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55169352-G-A

102378131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55169281-T-G

102378416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55169011-T-A

102378704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55168193-T-C

102378806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55168092-A-T

102379086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55167781-G-T

102379285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55167566-G-T

102379474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55167390-T-C

102379492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55167373-C-T

102380083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55166422-C-T

http://identifiers.org/hco/3/GRCh38#102382918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55157971-A-C

102383098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55157799-C-T

http://identifiers.org/hco/3/GRCh38#102383813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55157146-C-A

102383813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 5 prime UTR variant
orthologous variants: 55157146-C-T

http://identifiers.org/hco/3/GRCh38#102383820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55157139-C-A

102383891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 5 prime UTR variant
orthologous variants: 55157071-G-T

102383944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55157030-C-G

102383944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55157030-C-T

102383949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55157025-A-G

102384280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55156710-T-A

http://identifiers.org/hco/3/GRCh38#102384436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55156565-A-C

102384524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55156482-C-T

102388981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55150106-T-G

102389004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55150089-A-G

102389035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55150053-T-A

102389108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55149991-A-T

102389133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55149966-A-G

http://identifiers.org/hco/3/GRCh38#102389472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55149517-A-C

102389657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55149327-G-T

102389729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55149256-G-A

102389769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55149217-G-T

102389773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55149213-A-G

102390029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55148960-A-T

102390154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55148848-A-G

102390195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55148806-T-A

102390238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55148757-C-T

102390253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55148743-A-G

102390279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55148713-C-T

102390316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55148677-T-C

102390507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55148533-A-G

102390780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55147664-C-T

102390909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55147529-A-G

102390963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55147504-C-T

102391113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55147379-G-A

102391398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55146926-T-C

102393403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55140910-G-A

102393572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55140755-G-A

102394478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55139492-A-G

102394521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55139449-C-T

102394596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55139389-G-T

102394635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55139350-G-A

102394868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55139136-G-A

http://identifiers.org/hco/3/GRCh38#102395682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55138732-C-A

102395859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55138551-G-A

102395859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55138551-G-T

102396393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55138030-C-T

102396472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55137914-G-A

102396472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55137914-G-T

102396599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55137776-A-G

102396756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55137586-T-A

102397934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55137378-G-T

102398074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55137236-G-T

102398172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55137139-G-T

102398362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55136951-G-A

102398589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55136684-A-G

102398707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55136597-T-C

102398741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55136563-T-G

102398796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55136507-T-A

102398873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55136438-C-T

102398877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55136434-C-T

102398880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55136431-A-G

102398949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55136366-T-C

102399096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55135966-C-T

102399159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55135893-G-T

102399200-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55135850-T-A

102399200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55135850-T-C

102399373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55135584-C-T

102399493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55135464-C-T

102399545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55135412-A-G

102400267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55134895-T-C

102400334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55134832-T-G

102400704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55134481-A-T

102400922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, undefined
orthologous variants: 55134281-G-A

102400984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, undefined
orthologous variants: 55134219-T-G

102401154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55134044-C-T

102401185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55134016-A-G

102401230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55133993-C-G

102403536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55124554-A-T

102403594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55124499-T-C

102403647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55124446-T-C

102403895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55124218-C-T

102404083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55124049-A-G

102404120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55124012-G-A

102404239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55123892-G-A

102404493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55123626-A-G

102404493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55123626-A-T

102404557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55123565-C-T

102406269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55121192-G-A

102406537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55120894-G-C

102406619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55120817-C-T

102406853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55120584-A-G

102410339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55113016-T-G

102410995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55112386-T-C

102411044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55112345-T-C

102411328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55112079-T-C

102411416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55111991-A-G

http://identifiers.org/hco/3/GRCh38#102411464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55111947-A-C

102411643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55111785-A-G

102411665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55111766-A-G

102411722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55111732-T-C

102411759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55111693-T-C

102411789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55111672-C-T

102411851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55111615-G-A

102413045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55108974-A-G

102413122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55108896-A-T

102413128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55108890-A-T

102413165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55108852-G-A

http://identifiers.org/hco/3/GRCh38#102413589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55108011-C-A

102413607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55107994-T-A

102413741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55107834-T-C

http://identifiers.org/hco/3/GRCh38#102413826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55107760-C-A

102413900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55107718-C-T

102413979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55107646-T-C

102414908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55106713-T-C

102414984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55106521-T-C

102415195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55106333-C-T

102415239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55106288-A-G

102415313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55106210-G-A

102415326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55106197-G-T

102415762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55105643-T-C

102415777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55105628-A-G

102415955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55105453-G-C

102416041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55105367-T-C

102416372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55105034-T-C

102416442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55104962-A-G

102416465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55104939-G-A

102417033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55104375-A-T

102417408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55104028-A-G

102418035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55103414-T-C

http://identifiers.org/hco/3/GRCh38#102418078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55103363-C-A

102418078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 5 prime UTR variant
orthologous variants: 55103363-C-T

102418297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55103154-T-C

102418513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55102980-G-A

102418706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55102796-A-T

102418711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55102791-A-G

102418952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55102559-T-G

http://identifiers.org/hco/3/GRCh38#102419416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55102145-A-C

102419650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55101980-C-T

http://identifiers.org/hco/3/GRCh38#102419743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55101886-A-C

102420155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55101466-G-T

102420273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55101340-A-G

102420637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55100992-C-T

102421105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55100521-C-T

102421215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55100423-C-G

102421668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55099978-G-T

102421901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55099749-C-T

102421998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55099648-A-G

102422493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55099196-T-C

102422578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55099109-T-C

102422816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55098863-T-C

102422906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55098780-A-G

102423399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55097019-G-A

102427414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55095727-G-T

102427762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55095416-T-C

102427912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55095269-T-C

102427917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55095264-A-G

102427994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55095206-T-A

102428374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55094713-T-A

102428374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55094713-T-C

102428432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55094656-T-A

102430669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55093605-G-T

102430697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55093581-G-A

102430904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55093389-A-T

102430941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55093353-A-G

102430942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55093352-G-T

102430967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55093327-G-A

102430967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55093327-G-T

http://identifiers.org/hco/3/GRCh38#102430986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55093308-A-C

102431107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55093185-A-G

102431161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55093133-C-T

102431302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55092991-C-T

102431964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55092635-T-A

102432122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55092476-T-C

102432186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55092414-T-C

102432215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55092384-G-T

http://identifiers.org/hco/3/GRCh38#102432411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55092051-A-C

102432411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55092051-A-G

102432437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55092029-T-C

http://identifiers.org/hco/3/GRCh38#102432787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55091600-C-A

102432838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55091561-A-G

102432966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55091458-T-A

102433061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55091368-G-T

http://identifiers.org/hco/3/GRCh38#102433217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55091235-C-A

http://identifiers.org/hco/3/GRCh38#102433219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55091233-A-C

102433219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55091233-A-G

http://identifiers.org/hco/3/GRCh38#102433277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55091175-A-C

102433348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55091118-A-G

http://identifiers.org/hco/3/GRCh38#102434038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55090737-A-C

102434250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55090549-T-G

102434329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55090460-C-T

102436475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55089662-A-G

102436611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55089505-G-A

102436720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55089395-G-T

102436733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55089390-T-A

102436759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55089364-A-T

102436772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55089350-T-C

102436800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55089321-A-G

102436891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55089248-G-C

http://identifiers.org/hco/3/GRCh38#102436896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55089242-A-C

102436896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55089242-A-G

102436926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55089212-G-A

102436926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55089212-G-T

102436991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55089178-T-C

102437003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55089166-A-G

102437003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55089166-A-T

102437008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55089161-T-C

102437102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55089065-G-T

102437114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55089053-G-A

102437114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55089053-G-T

102437156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55089011-T-C

102437157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55089010-A-G

102437873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55088298-T-C

102438045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55088152-C-T

102438373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55087829-G-A

102438396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55087806-G-A

102438396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55087806-G-C

102438396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55087806-G-T

102438410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55087793-C-T

102438434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55087734-A-T

102438450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55087697-G-A

102438512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: missense variant
orthologous variants: 55087636-C-T

102438663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55087484-T-A

102438663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55087484-T-G

102439091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55087043-T-A

102439216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55086923-T-A

102439531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55086625-G-A

102439631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55086516-G-A

102439733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55086415-C-T

102439835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55086316-T-G

102440070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55086176-G-A

102440284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55085971-A-T

102440371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55085883-G-T

102440557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55085703-G-C

102440690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55085571-G-A

102440699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55085561-T-A

102440699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55085561-T-G

102440723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55085530-G-T

102440731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55085522-G-A

102440731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55085522-G-T

102440966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55085352-G-A

http://identifiers.org/hco/3/GRCh38#102441481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55084672-C-A

102441624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55084522-C-T

http://identifiers.org/hco/3/GRCh38#102441665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55084495-A-C

102441718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55084448-A-G

102441820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55084358-T-A

102442461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55083949-G-A

102442479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55083932-G-C

102442479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55083932-G-T

http://identifiers.org/hco/3/GRCh38#102442807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55083603-C-A

102442918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55083491-C-T

102442926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55083483-A-G

102442983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55083432-A-G

102443107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55083301-C-T

102443375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55083071-A-G

102443910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55081835-T-C

http://identifiers.org/hco/3/GRCh38#102444049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55081697-A-C

102444092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55081650-C-T

102444673-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55081053-T-A

102444673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55081053-T-C

102445012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55080749-T-C

102445019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55080742-G-A

102445020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55080741-G-A

102445556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55080253-C-T

http://identifiers.org/hco/3/GRCh38#102445820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55079986-C-A

http://identifiers.org/hco/3/GRCh38#102445891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55079905-A-C

http://identifiers.org/hco/3/GRCh38#102446461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55079586-C-A

102446499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55079544-A-T

102447000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55077968-A-G

102447031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55077937-T-C

102447529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron_variant, undefined
orthologous variants: 55077775-A-G

102447631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55077669-A-G

102447692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55077602-A-G

102447743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55077548-T-G

102447905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55077382-G-A

102448076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55077195-A-G

102448173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55077100-G-A

102448215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55077057-C-G

102448626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55076588-T-G

102448794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55076406-A-G

102448931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55076052-C-T

102448932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55076051-A-G

102448978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55075935-G-T

102449043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55075858-C-T

102449203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55075709-C-G

http://identifiers.org/hco/3/GRCh38#102449309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55075601-C-A

102449309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55075601-C-G

102449309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55075601-C-T

http://identifiers.org/hco/3/GRCh38#102450029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55075396-A-C

102450512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55074972-A-G

http://identifiers.org/hco/3/GRCh38#102450535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55074963-C-A

102450751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55074799-T-C

102450751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55074799-T-G

102450885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55074646-A-G

102450901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55074627-A-G

102450961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55074571-T-C

102451040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55074500-T-G

102451293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55074277-C-T

102451294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55074276-T-G

102451362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55074209-T-G

102451584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55073993-T-C

http://identifiers.org/hco/3/GRCh38#102451664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55073921-C-A

102451664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55073921-C-T

102451675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55073910-C-G

http://identifiers.org/hco/3/GRCh38#102451798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55073771-C-A

102451798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55073771-C-G

102451798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55073771-C-T

102451812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55073764-G-A

102451941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55073651-G-A

102451961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55073631-T-G

102452111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55073506-G-A

102452111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55073506-G-T

102452231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55073388-T-C

102452656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55072387-G-T

102452705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55072338-T-C

102452725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55072322-C-T

102452847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55072229-A-G

102452847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55072229-A-T

102452872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55072205-T-G

102453101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: missense variant
orthologous variants: 55071967-A-G

http://identifiers.org/hco/3/GRCh38#102453193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55071875-C-A

102453193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55071875-C-G

http://identifiers.org/hco/3/GRCh38#102453200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55071868-C-A

102453200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55071868-C-T

102453216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55071852-G-T

102453240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55071823-A-G

102453269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55071794-G-A

102453407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55071659-G-A

102453544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55071549-G-C

102453767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55071331-T-G

http://identifiers.org/hco/3/GRCh38#102454315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55070804-A-C

102454325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55070794-A-G

102454877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55070349-A-G

102454883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55070343-A-G

102454888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55070338-T-C

102455044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55070146-T-A

102455266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55069929-G-A

102455274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55069921-T-C

102455421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55069783-T-A

102455480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55069743-A-G

102455520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55069703-C-T

102455534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55069689-T-C

102455643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55069586-T-C

102455921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55069052-A-G

102455999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55068978-A-G

http://identifiers.org/hco/3/GRCh38#102456051-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55068937-A-C

102456051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55068937-A-G

http://identifiers.org/hco/3/GRCh38#102456069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55068907-C-A

102456069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55068907-C-G

102456069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55068907-C-T

102456102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55068871-T-C

102456151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55068822-T-C

102456168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55068805-T-C

102456209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: missense variant
orthologous variants: 55068764-G-T

102456233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: missense variant
orthologous variants: 55068740-C-T

http://identifiers.org/hco/3/GRCh38#102456274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55068699-C-A

102456280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: missense variant
orthologous variants: 55068693-C-G

http://identifiers.org/hco/3/GRCh38#102456284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55068689-C-A

102456284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: missense variant
orthologous variants: 55068689-C-T

102456337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: missense variant
orthologous variants: 55068636-C-T

http://identifiers.org/hco/3/GRCh38#102456418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55068554-C-A

102456418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55068554-C-T

102456667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55068073-G-T

102456810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55067934-T-G

102456864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55067890-G-A

102456936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55067836-C-T

102457141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55067642-G-A

102457200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55067594-A-G

102457333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55067481-A-G

102457582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55067246-G-A

102457655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55067173-A-G

102457754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55067069-G-A

102457917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55066906-T-C

102457944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55066879-G-T

102457957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55066866-T-C

102458099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55066724-T-C

http://identifiers.org/hco/3/GRCh38#102458119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55066654-A-C

102458149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55066624-A-G

102458211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55066571-T-C

102458423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55066360-C-T

102458618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55066166-A-G

102458628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55066156-A-G

102458662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55066122-G-A

102458970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55065708-G-A

102458982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55065698-C-T

102459075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55065643-G-A

102459077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55065641-G-A

102459077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55065641-G-C

102459077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55065641-G-T

102459149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55065535-T-A

102459149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55065535-T-C

102459246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55065353-G-A

102459246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55065353-G-T

102459282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55065295-A-T

102459370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55065184-A-G

102459828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55064656-A-G

102459836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55064648-T-C

102459934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55064561-G-A

102460184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55064334-T-C

102460741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55063915-T-A

102460741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55063915-T-C

http://identifiers.org/hco/3/GRCh38#102460897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55063759-A-C

102461308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55062780-T-C

102461569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55062418-G-C

102461848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55062214-G-A

102461953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55062114-T-C

102462081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55061990-T-G

102462123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55061947-G-T

102462174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55061900-T-G

102462242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55061838-G-T

102462437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55061650-G-A

102462437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55061650-G-T

102462832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55061156-C-G

102463045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55060868-G-A

102463286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55060663-C-T

102463602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55060378-T-C

http://identifiers.org/hco/3/GRCh38#102464241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55060195-C-A

102464277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55060166-T-C

102464320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55060123-T-C

102464355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55060086-T-C

102464420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55060034-G-C

102464451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55060003-C-T

102464574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55059879-G-C

http://identifiers.org/hco/3/GRCh38#102464600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55059853-C-A

http://identifiers.org/hco/3/GRCh38#102464743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55059705-A-C

102465162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55059285-T-C

http://identifiers.org/hco/3/GRCh38#102465664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55058818-A-C

102465665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55058817-T-C

http://identifiers.org/hco/3/GRCh38#102467424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55055271-C-A

102467424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55055271-C-T

102467643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55055074-T-C

102467661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55055056-A-G

102467702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55055014-T-C

102467930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55054933-C-T

102468196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55054713-A-G

102468250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55054673-G-A

102468730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55054270-A-G

102468776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55054217-T-C

102468835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55054155-G-A

102468867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55054126-T-C

102468887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55054105-G-A

102468887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55054105-G-T

102468888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55054104-G-A

102468907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55054085-T-C

http://identifiers.org/hco/3/GRCh38#102469013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55053978-C-A

102469013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: missense variant
orthologous variants: 55053978-C-T

102469072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: synonymous variant
orthologous variants: 55053919-C-T

102469586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55053455-C-T

102469762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55053317-A-G

102469797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55053283-A-G

102470433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: missense variant
orthologous variants: 55052638-A-T

102470466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: missense variant
orthologous variants: 55052605-G-A

102470466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: missense variant
orthologous variants: 55052605-G-T

102470514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55052558-C-G

102470588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55052489-T-C

http://identifiers.org/hco/3/GRCh38#102470598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55052479-C-A

102470598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55052479-C-T

102471376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55052188-T-G

102471650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55051962-G-T

102471667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55051947-T-C

http://identifiers.org/hco/3/GRCh38#102471703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55051910-A-C

102471847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55051806-T-C

102471847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55051806-T-G

102472061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55051599-C-G

102472136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55051534-C-G

102472140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55051530-T-C

102472610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55051378-C-T

102472669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55051320-G-C

http://identifiers.org/hco/3/GRCh38#102472823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55051170-C-A

http://identifiers.org/hco/3/GRCh38#102473511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55050688-C-A

102473571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55050625-T-C

102473717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55050511-A-G

102473717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55050511-A-T

102473899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55050336-A-G

102473991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55050245-T-C

102474082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55050151-T-G

102474367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55049884-G-C

102474603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55049669-A-T

102474915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55049351-G-A

102474980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55049293-G-A

102474980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55049293-G-C

102475138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55049154-A-T

102475232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55049070-G-A

102475309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55048998-G-A

102475309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55048998-G-T

102475373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55048868-T-A

102475397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55048844-T-C

102475934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55048322-A-G

102475991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55048265-A-G

102476088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55048168-A-G

102476256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55048003-A-G

102476324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55047961-G-T

102476651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55047641-C-G

102476715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55047578-C-G

102476995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55047341-C-T

102477103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55047230-T-C

102477178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55047156-A-G

102477186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55047149-T-C

http://identifiers.org/hco/3/GRCh38#102477316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55047011-C-A

102477316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55047011-C-T

102477332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55046998-G-A

102477332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55046998-G-T

http://identifiers.org/hco/3/GRCh38#102477333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55046997-C-A

102477333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55046997-C-T

102477371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55046964-G-A

102477371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55046964-G-T

102477382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55046951-G-A

102477382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55046951-G-T

102477431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: intron variant
orthologous variants: 55046905-T-C

102477511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: missense variant
orthologous variants: 55046825-C-G

102477710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 3 prime UTR variant
orthologous variants: 55046630-A-G

102477944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 3 prime UTR variant
orthologous variants: 55046392-G-T

102477946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 3 prime UTR variant
orthologous variants: 55046390-G-A

102477964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 3 prime UTR variant
orthologous variants: 55046372-A-G

102478160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 3 prime UTR variant
orthologous variants: 55046176-T-C

102478173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 3 prime UTR variant
orthologous variants: 55046163-T-C

102478301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 3 prime UTR variant
orthologous variants: 55046036-A-G

102478449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 3 prime UTR variant
orthologous variants: 55045909-T-A

102478449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 3 prime UTR variant
orthologous variants: 55045909-T-C

102478449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 3 prime UTR variant
orthologous variants: 55045909-T-G

102478505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 3 prime UTR variant
orthologous variants: 55045844-A-G

http://identifiers.org/hco/3/GRCh38#102478598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55045748-C-A

102478598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 3 prime UTR variant
orthologous variants: 55045748-C-T

http://identifiers.org/hco/3/GRCh38#102478727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55045608-C-A

102478727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 3 prime UTR variant
orthologous variants: 55045608-C-T

102478766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 3 prime UTR variant
orthologous variants: 55045553-C-T

http://identifiers.org/hco/3/GRCh38#102478790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55045528-A-C

102478790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 3 prime UTR variant
orthologous variants: 55045528-A-G

102479314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 3 prime UTR variant
orthologous variants: 55045026-T-C

102479335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 3 prime UTR variant
orthologous variants: 55045005-A-G

102479573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27022
most severe consequence: 3 prime UTR variant
orthologous variants: 55044736-T-G