186266443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45714839-C-T

186266453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45714829-C-G

186266505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45714772-C-T

186266557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45714726-A-G

186266565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45714718-A-G

http://identifiers.org/hco/4/GRCh38#186266582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45714701-C-A

186266582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45714701-C-G

186266692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45714580-T-C

186266739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45714471-T-A

186266739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45714471-T-C

186266777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, undefined
orthologous variants: 45714433-T-A

186266805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, undefined
orthologous variants: 45714411-G-C

186266813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45714403-G-A

186266862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45714354-C-T

186266863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45714353-G-A

186266937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45714291-A-G

186267001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45714242-A-G

186267001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45714242-A-T

186267023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45714220-T-C

http://identifiers.org/hco/4/GRCh38#186267024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45714219-A-C

http://identifiers.org/hco/4/GRCh38#186267040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#45714203-C-A

186267069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, undefined
orthologous variants: 45714181-G-C

http://identifiers.org/hco/4/GRCh38#186267073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#45714177-C-A

186267073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, undefined
orthologous variants: 45714177-C-T

http://identifiers.org/hco/4/GRCh38#186267250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45713615-A-C

186267250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45713615-A-G

186267320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45713548-G-A

186267379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45713466-G-A

186267424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45713430-A-G

186267445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45713409-G-T

186267620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45713133-A-G

186267635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45713115-C-T

http://identifiers.org/hco/4/GRCh38#186267653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45713097-C-A

186271475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45708520-A-G

186271475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45708520-A-T

186271496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45708499-A-G

http://identifiers.org/hco/4/GRCh38#186271527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45708487-C-A

186271527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45708487-C-T

186271536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45708478-T-C

186271588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45708427-A-G

186271662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: missense variant
orthologous variants: 45708348-A-G

186271678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: missense variant
orthologous variants: 45708332-G-T

http://identifiers.org/hco/4/GRCh38#186271683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45708327-A-C

186271752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: missense variant
orthologous variants: 45708258-T-C

186271814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45708181-G-T

186271905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45708092-T-C

186271906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45708091-T-C

186272568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45706990-T-C

186272634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45706928-G-T

186272663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45706914-G-A

186272677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45706900-G-C

http://identifiers.org/hco/4/GRCh38#186272850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45706392-C-A

186272872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45706369-A-G

http://identifiers.org/hco/4/GRCh38#186272955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45706287-C-A

186272955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45706287-C-T

186272979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45706263-T-C

http://identifiers.org/hco/4/GRCh38#186273014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45706244-C-A

186273014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45706244-C-T

186273037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45706222-C-T

http://identifiers.org/hco/4/GRCh38#186273221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45706008-C-A

186273221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706008-C-T

186273234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705995-A-G

186273982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705360-G-A

186273982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705360-G-T

186273985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705357-G-T

186273986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705356-A-T

186274175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45705153-G-C

186274175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45705153-G-T

186274251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45705077-G-A

186274251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45705077-G-T

186274320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45704998-T-A

186274320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45704998-T-C

186274361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45704960-G-A

http://identifiers.org/hco/4/GRCh38#186274563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45704186-A-C

186274563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45704186-A-G

186274565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45704184-T-C

186274670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45704070-G-C

186274670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45704070-G-T

186274678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45704055-A-G

186274678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45704055-A-T

186274679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45704054-C-T

186274704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45704029-C-T

186274738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45703994-C-G

186274968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45703680-A-G

186274976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45703672-A-T

186274977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45703671-G-A

186274977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45703671-G-C

186274983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45703665-T-A

186274983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45703665-T-G

186275008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45703640-A-G

186275619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45703387-C-T

186275630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45703367-C-T

186275633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45703364-C-G

http://identifiers.org/hco/4/GRCh38#186275655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45703343-C-A

186275655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45703343-C-T

186275673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45703325-G-A

http://identifiers.org/hco/4/GRCh38#186275677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45703321-C-A

186275677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45703321-C-G

186275697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45703285-T-C

186275764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45703224-T-C

186275937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45703050-T-C

186275946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45703032-G-T

http://identifiers.org/hco/4/GRCh38#186275984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45702994-C-A

186275984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45702994-C-T

186276176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45702758-A-G

http://identifiers.org/hco/4/GRCh38#186276204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45702727-C-A

186276222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45702708-G-A

186276222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45702708-G-C

186276222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45702708-G-T

186276251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, missense_variant
orthologous variants: 45702679-C-T

http://identifiers.org/hco/4/GRCh38#186276258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45702672-C-A

186276258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, missense_variant
orthologous variants: 45702672-C-T

http://identifiers.org/hco/4/GRCh38#186276326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45702604-A-C

186276368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, missense_variant
orthologous variants: 45702562-G-A

http://identifiers.org/hco/4/GRCh38#186276374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45702556-C-A

186276374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, missense_variant
orthologous variants: 45702556-C-T

186276396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45702534-G-A

186276426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45702505-T-C

http://identifiers.org/hco/4/GRCh38#186276430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45702500-A-C

186276430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45702500-A-G

186279676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45702452-G-A

186279685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45702443-A-G

186279716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45702412-G-C

186279758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45702369-C-T

186279860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45702304-G-A

186279860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45702304-G-T

186279882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45702284-G-A

186279882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45702284-G-C

186280176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45701991-T-C

186280203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45701961-A-T

186280315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: missense variant
orthologous variants: 45701849-C-G

http://identifiers.org/hco/4/GRCh38#186280364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45701800-A-C

http://identifiers.org/hco/4/GRCh38#186280371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45701793-C-A

186280467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 45701702-A-G

186280580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 45701589-G-A

186280583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45701586-G-A

186280608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45701569-T-C

186281773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45700913-C-G

186281839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45700849-T-C

186281839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45700849-T-G

186281855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45700833-G-A

186281855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45700833-G-C

186281856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45700832-A-T

186281857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45700831-G-A

186281857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45700831-G-T

186281954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, missense_variant
orthologous variants: 45700739-G-A

186281968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, stop_gained
orthologous variants: 45700725-G-A

186281968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, missense_variant
orthologous variants: 45700725-G-T

186281983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, stop_retained_variant
orthologous variants: 45700711-A-G

186282063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45700634-G-A

186282063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45700634-G-T

186282064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45700633-G-A

186282064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45700633-G-T

186282094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45700605-A-G

186282141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45700562-A-G

186282156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45700548-A-G

http://identifiers.org/hco/4/GRCh38#186282183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45700521-C-A

186282183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45700521-C-T

186282275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45700428-A-G

186282303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45700404-A-G

http://identifiers.org/hco/4/GRCh38#186282327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45700385-C-A

http://identifiers.org/hco/4/GRCh38#186282405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45700328-C-A

186282410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45700321-T-C

186282413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45700318-T-C

http://identifiers.org/hco/4/GRCh38#186282418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45700313-A-C

186282443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45700288-A-T

186282483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45700248-T-C

http://identifiers.org/hco/4/GRCh38#186282593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45700127-A-C

186282658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45700065-T-A

186284085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 45699948-G-A

http://identifiers.org/hco/4/GRCh38#186284115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45699918-A-C

186284115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 45699918-A-T

186284163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 45699870-G-A

186284163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 45699870-G-T

186284166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: missense variant
orthologous variants: 45699867-A-G

186284226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: missense variant
orthologous variants: 45699816-C-G

186284241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: missense variant
orthologous variants: 45699801-G-A

186284431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45699610-C-T

186285100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45699297-G-T

186285159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45699241-G-A

186285452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45699004-G-A

186285537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45698924-G-A

186285537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45698924-G-T

186285650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: synonymous variant
orthologous variants: 45698827-T-A

186285659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: synonymous variant
orthologous variants: 45698818-G-A

186285659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: missense variant
orthologous variants: 45698818-G-C

186285848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45698637-T-C

http://identifiers.org/hco/4/GRCh38#186285909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45698590-C-A

http://identifiers.org/hco/4/GRCh38#186285919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45698580-C-A

186285919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45698580-C-T

186285940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45698555-T-A

186285940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45698555-T-C

http://identifiers.org/hco/4/GRCh38#186285963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45698534-C-A

186286000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45696817-T-C

186286012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45696805-G-A

186286012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45696805-G-T

186286078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45696742-G-A

186286078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45696742-G-C

186286079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron variant
orthologous variants: 45696741-G-C

186286135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45696700-A-G

186286200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45696638-C-T

186286241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45696591-G-A

186286241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45696591-G-C

186286241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45696591-G-T

http://identifiers.org/hco/4/GRCh38#186286243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45696589-C-A

186286243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45696589-C-T

http://identifiers.org/hco/4/GRCh38#186286244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45696588-A-C

186286244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45696588-A-G

186286244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45696588-A-T

186286248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45696584-G-A

186286248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45696584-G-T

186286301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45696536-A-T

186286324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45696513-A-G

186286342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45696495-G-A

186286342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45696495-G-T

186286461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45695950-A-G

186286500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45695911-A-G

http://identifiers.org/hco/4/GRCh38#186286597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45695802-A-C

186286779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45695658-T-G

186286902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45695538-C-T

186286917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45695522-G-T

186287617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45695440-T-C

186287625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45695432-T-C

186287725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45695350-G-A

http://identifiers.org/hco/4/GRCh38#186287773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45695302-C-A

186287821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45695254-A-G

186288197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45694855-C-G

186288251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45694844-A-G

186288299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45694796-A-G

186288304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45694791-G-A

186288304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45694791-G-T

186288340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45694755-A-G

186288348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45694747-G-A

186288576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45694521-T-G

186288622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45694473-C-T

http://identifiers.org/hco/4/GRCh38#186288623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45694472-C-A

186288623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45694472-C-T

186288629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45694466-G-A

http://identifiers.org/hco/4/GRCh38#186288688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45694400-C-A

186288695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45694395-G-A

186288695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45694395-G-C

http://identifiers.org/hco/4/GRCh38#186288696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45694394-C-A

http://identifiers.org/hco/4/GRCh38#186288702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45694388-C-A

186288702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45694388-C-T

http://identifiers.org/hco/4/GRCh38#186288713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45694377-C-A

186288713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45694377-C-T

186288719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45694371-A-T

186288771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45694333-T-A

186288771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45694333-T-C

186288908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45694219-T-C

186288908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45694219-T-G

186289232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45692959-A-G

186289233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45692958-G-A

186289502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45692681-A-T

186289584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3529
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45692625-T-C