http://identifiers.org/hco/2/GRCh38#84460013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73224938-C-A

http://identifiers.org/hco/2/GRCh38#84460042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#73224909-C-A

http://identifiers.org/hco/2/GRCh38#84516303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#73198828-A-C

84516349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, undefined
orthologous variants: 73198780-A-G

84516364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73198765-A-G

http://identifiers.org/hco/2/GRCh38#84516398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73198729-C-A

84516398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73198729-C-T

84516409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73198721-G-T

84516413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, undefined
orthologous variants: 73198717-G-A

84516438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, undefined
orthologous variants: 73198687-T-G

http://identifiers.org/hco/2/GRCh38#84516460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#73198663-C-A

84516460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 73198663-C-G

84516460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 73198663-C-T

84516467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 73198656-G-T

84516551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 73198572-G-T

84516628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73198509-G-A

84516628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73198509-G-T

http://identifiers.org/hco/2/GRCh38#84516719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#73198436-C-A

84516948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73198283-G-A

84517704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73196883-G-T

84517709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73196878-A-G

http://identifiers.org/hco/2/GRCh38#84517731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73196847-C-A

84517759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73196820-T-G

84517765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73196814-C-T

84525565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 73185689-C-T

84525741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73185525-A-G

http://identifiers.org/hco/2/GRCh38#84525777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73185491-A-C

http://identifiers.org/hco/2/GRCh38#84525802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73185469-C-A

84525802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73185469-C-T

84525803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73185468-A-G

84525803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73185468-A-T

84525805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73185466-A-G

http://identifiers.org/hco/2/GRCh38#84526005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73185213-A-C

84526005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73185213-A-G

84526081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73185135-G-A

84528767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73183032-A-G

84528961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 73182878-G-C

http://identifiers.org/hco/2/GRCh38#84529006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73182833-C-A

84529006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 73182833-C-T

84529153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 73182686-A-G

http://identifiers.org/hco/2/GRCh38#84529300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73182533-C-A

84529872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73181759-T-C

84529933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73181709-T-C

84530274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73181522-G-A

84530427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73181394-G-A

84530579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73181231-G-A

84530702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73181088-G-T

84530764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73181042-A-G

84530765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73181041-A-G

84530766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73181034-C-T

84531731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73180778-G-A

84531731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73180778-G-C

84532052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73180427-A-G

http://identifiers.org/hco/2/GRCh38#84532170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73180312-A-C

84532193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73180288-A-G

http://identifiers.org/hco/2/GRCh38#84532263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73180212-C-A

84532264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73180211-A-G

84541482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73176157-T-A

http://identifiers.org/hco/2/GRCh38#84541495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73176144-A-C

84541664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73175986-A-T

84541712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73175940-G-A

84541748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73175906-T-C

84541803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73175855-A-T

84541880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73175783-A-T

84542033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73175115-G-A

84542053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73175100-C-T

84542062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73175091-G-A

84542118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73175044-A-G

http://identifiers.org/hco/2/GRCh38#84542335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73174344-C-A

84543395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73174184-G-A

http://identifiers.org/hco/2/GRCh38#84543536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73174048-A-C

84543573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73174002-A-G

84543726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73173897-T-G

84543742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73173881-A-G

84543782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73173850-A-G

84544537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73172501-T-A

84545609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73171762-C-T

84545610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73171761-G-A

http://identifiers.org/hco/2/GRCh38#84545617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73171754-A-C

84545642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73171729-C-G

84545699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73171673-C-T

84546532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73170796-T-C

84546606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73170725-A-G

84546777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73170484-G-A

http://identifiers.org/hco/2/GRCh38#84546970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73170308-A-C

84546970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73170308-A-G

84547074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73170240-T-A

http://identifiers.org/hco/2/GRCh38#84547163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73170119-C-A

84547163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73170119-C-G

84547409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 73169874-A-T

84547422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73169861-A-G

84547432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73169851-C-T

84547483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73169803-A-G

84547484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 73169802-A-G

84547522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 73169764-G-C

84547522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 73169764-G-T

http://identifiers.org/hco/2/GRCh38#84547604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73169682-C-A

84547604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 73169682-C-T

84547620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 73169666-G-A

84547620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 73169666-G-C

84547682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73169619-G-T

84548162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73169529-G-T

http://identifiers.org/hco/2/GRCh38#84548235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73169462-A-C

84548235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73169462-A-G

84548247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73169452-T-C

84548255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73169444-T-A

84549644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73168843-A-G

http://identifiers.org/hco/2/GRCh38#84549713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73168774-A-C

84549716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73168771-A-G

84549817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73168682-T-C

84549887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 73168617-A-G

84549887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 73168617-A-T

84549905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73168599-G-A

84549905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73168599-G-T

84549933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73168571-T-A

84549969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73168535-A-G

84550004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73168500-G-A

84550004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73168500-G-C

http://identifiers.org/hco/2/GRCh38#84552834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73167519-C-A

84552834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73167519-C-T

84552884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73167465-T-A

84552884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73167465-T-C

84552957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73167392-C-T

84553035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 73167314-G-A

84553035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 73167314-G-C

84553035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 73167314-G-T

84553082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73167265-A-G

http://identifiers.org/hco/2/GRCh38#84553117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73167230-A-C

84553117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73167230-A-G

84557107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73166190-C-T

84557707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73165535-T-C

84557707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73165535-T-G

84557852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73165394-G-A

84557885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73165361-G-A

84557939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73165307-T-C

84558023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73165223-A-G

84558255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73165006-A-G

84558395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73164932-G-T

84558439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73164886-A-G

84558928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73163676-A-G

http://identifiers.org/hco/2/GRCh38#84573527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73158748-C-A

84573545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 73158730-A-G

http://identifiers.org/hco/2/GRCh38#84573563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/6/GRCm39#73158712-C-A

84573563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: non_coding_transcript_exon_variant, stop_gained, synonymous_variant
orthologous variants: 73158712-C-T

84573635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73158645-G-A

84573635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73158645-G-T

84573641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73158639-T-C

http://identifiers.org/hco/2/GRCh38#84573690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73158589-C-A

84573690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73158589-C-T

84573773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73158509-A-T

84573847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73158440-T-G

84574026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73158272-A-T

84577187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73156911-T-C

84577235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73156863-T-G

http://identifiers.org/hco/2/GRCh38#84577391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73156707-C-A

84577429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73156669-A-G

84578468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73156224-C-T

84578469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73156223-G-A

84579134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73155939-C-T

84579221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73155852-G-A

84579365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73155700-C-T

84579578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73155496-A-G

http://identifiers.org/hco/2/GRCh38#84579743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73155334-C-A

http://identifiers.org/hco/2/GRCh38#84579789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73152474-C-A

http://identifiers.org/hco/2/GRCh38#84579794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73152469-A-C

84579794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73152469-A-G

84579794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73152469-A-T

84580558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73151929-G-A

84580558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73151929-G-T

84580928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73151570-C-T

84580947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73151551-G-T

84583247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73150987-G-A

84583348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73150897-C-T

84583462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73150703-T-C

http://identifiers.org/hco/2/GRCh38#84583965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73150572-C-A

84583965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73150572-C-T

84584304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73150244-A-G

84584304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73150244-A-T

84584348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73150197-T-A

http://identifiers.org/hco/2/GRCh38#84584420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73150145-C-A

84584420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73150145-C-T

http://identifiers.org/hco/2/GRCh38#84584464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73150101-C-A

84584480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73150085-T-A

http://identifiers.org/hco/2/GRCh38#84584520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73150047-A-C

http://identifiers.org/hco/2/GRCh38#84584759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73149827-C-A

84584787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73149790-A-G

84584793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73149789-A-G

84584975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73149596-T-C

84585044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73149509-A-G

84585044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73149509-A-T

http://identifiers.org/hco/2/GRCh38#84585212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73149331-C-A

84588136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73148365-T-G

http://identifiers.org/hco/2/GRCh38#84588429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73146503-A-C

84588720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73146038-G-A

84588720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73146038-G-T

84588731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73146023-G-A

84588731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73146023-G-T

84588735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73146019-T-A

84588754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73146000-T-G

http://identifiers.org/hco/2/GRCh38#84588786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73145977-A-C

http://identifiers.org/hco/2/GRCh38#84588962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73145802-C-A

84588962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 73145802-C-T

84589038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73145727-T-A

84589047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73145718-A-G

84589052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73145717-T-C

http://identifiers.org/hco/2/GRCh38#84589067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73145706-C-A

84589067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73145706-C-G

84589067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73145706-C-T

84589267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73145209-A-G

84589738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73145072-T-A

84589738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73145072-T-G

84590030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73144888-G-A

http://identifiers.org/hco/2/GRCh38#84590066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73144851-A-C

http://identifiers.org/hco/2/GRCh38#84590077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73144840-A-C

84590079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73144838-G-A

84590090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73144827-T-C

84593229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73142125-T-C

84593658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73140853-A-G

http://identifiers.org/hco/2/GRCh38#84593779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73140765-A-C

84593808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73140727-T-G

http://identifiers.org/hco/2/GRCh38#84593945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73140600-C-A

84593945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73140600-C-T

84594299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73139863-G-A

84594299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73139863-G-T

http://identifiers.org/hco/2/GRCh38#84594311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73139851-A-C

84594311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73139851-A-G

84594388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73139774-G-T

84594618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73139555-A-T

84594649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73139538-G-A

84594681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73139480-G-T

84594788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73139376-C-G

84594819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73139344-G-A

84594824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73139339-G-T

84595466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73138150-C-T

84595533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73138111-T-C

84595588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73138046-A-G

84595588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73138046-A-T

84595667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73137967-C-T

http://identifiers.org/hco/2/GRCh38#84595875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73137798-C-A

84596103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73137639-G-T

84596196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73137546-T-C

84603039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73137366-A-G

84603050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73137355-A-G

84603107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73137294-G-A

84603112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73137288-G-C

84603143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73137238-T-C

84604537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73136081-G-A

84604739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73135700-T-C

http://identifiers.org/hco/2/GRCh38#84604943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73135482-C-A

84605011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73135383-T-C

84605029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73135365-C-T

84605600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 73135116-A-G

84605600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 73135116-A-T

84605642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73135004-T-A

84605709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73134834-A-G

84606020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73134532-A-G

84606109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73134479-A-T

84606194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73134410-A-G

84606294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73134327-C-T

84606352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73134294-T-C

84606355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73134291-G-A

84606481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73134195-G-A

84606553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73134167-G-C

http://identifiers.org/hco/2/GRCh38#84606634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73134132-C-A

84606727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73134045-G-C

84606979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73133438-C-G

84606979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73133438-C-T

84607102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 73133315-A-G

http://identifiers.org/hco/2/GRCh38#84607123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73133294-A-C

84607123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73133294-A-G

84607123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73133294-A-T

84611356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73132724-C-T

84611452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73132628-T-A

http://identifiers.org/hco/2/GRCh38#84611569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73132518-C-A

84611569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73132518-C-G

84611600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73132488-T-G

http://identifiers.org/hco/2/GRCh38#84611602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73132486-A-C

84611602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73132486-A-G

84611604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73132484-G-T

84611620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73132468-A-G

84611620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73132468-A-T

84611629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73132459-T-G

84612496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73131535-A-G

84613141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73131237-G-A

84613159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, undefined
orthologous variants: 73131219-G-A

84613161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, undefined
orthologous variants: 73131217-G-A

84613499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, undefined
orthologous variants: 73130788-A-G

84616773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73129861-T-C

84616801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73129826-T-C

84616819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73129796-A-G

84616819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73129796-A-T

84616969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73129663-G-A

84616969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73129663-G-T

84617839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73129451-C-G

84617926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73129375-A-T

84617934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73129367-C-T

84618081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73129209-A-G

84619093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73129119-T-C

84619522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73128841-G-A

http://identifiers.org/hco/2/GRCh38#84619551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73128812-C-A

84619551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73128812-C-T

84619654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73128723-A-G

84619660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73128717-A-G

84619833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73128543-G-C

84619836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73128540-A-G

84619932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73128443-A-G

http://identifiers.org/hco/2/GRCh38#84620028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73128329-C-A

84620042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73128315-G-A

84620042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73128315-G-T

http://identifiers.org/hco/2/GRCh38#84620264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73128112-A-C

84620388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73128025-T-A

84620480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73127946-G-A

84620574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73127909-G-A

84620846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73126853-C-T

84620988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73126709-T-C

84621044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73126662-G-A

84621044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73126662-G-T

84621084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73126645-A-G

84621105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73126624-T-C

84621105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73126624-T-G

84621136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73126593-T-G

84621142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73126587-T-A

84621227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73126507-G-A

84621363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 73126338-A-G

84621383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73126284-T-C

84621424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73126202-A-G

http://identifiers.org/hco/2/GRCh38#84621444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73126182-C-A

84621517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73126112-A-G

84621517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73126112-A-T

84621579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73126044-T-C

84621683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73125953-A-G

84621684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73125952-A-G

84623303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73122876-G-A

84623362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73122816-G-A

84623661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73122609-C-T

84623692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73122580-C-T

84623824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73122469-A-G

84623891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73122291-C-G

http://identifiers.org/hco/2/GRCh38#84623910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73122268-A-C

84624028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73122160-T-C

84624077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73122093-C-G

84624077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73122093-C-T

84624426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73121846-T-C

http://identifiers.org/hco/2/GRCh38#84624501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73121760-C-A

84624501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: synonymous variant
orthologous variants: 73121760-C-T

84624573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73121688-T-C

http://identifiers.org/hco/2/GRCh38#84624759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73121540-A-C

84624765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73121533-G-A

84624782-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73121516-T-A

84624792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73121506-T-C

84624806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73121494-A-G

84624873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73121183-T-G

84624880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73121175-G-A

84624887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73121167-C-T

84624950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73121104-G-A

84624950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73121104-G-C

84624950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73121104-G-T

84625084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73120965-T-C

84625193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73120873-G-A

84625193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73120873-G-C

84625193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73120873-G-T

84633717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73120371-C-T

84633750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73120355-A-T

84633765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73120340-G-A

84633765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73120340-G-T

http://identifiers.org/hco/2/GRCh38#84633784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73120321-A-C

84633891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73120200-C-T

84633915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73120176-T-C

84633990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73120119-T-C

84634097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73119796-G-A

84634097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73119796-G-T

http://identifiers.org/hco/2/GRCh38#84634171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73119728-A-C

84634195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73119708-A-G

84634205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73119700-C-T

84634213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73119682-G-C

http://identifiers.org/hco/2/GRCh38#84634358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73119529-C-A

84634358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73119529-C-T

84634510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73119373-G-T

http://identifiers.org/hco/2/GRCh38#84634513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73119370-C-A

84634513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73119370-C-T

84634636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73119247-G-A

84634636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73119247-G-T

http://identifiers.org/hco/2/GRCh38#84634648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73119235-C-A

http://identifiers.org/hco/2/GRCh38#84634649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73119234-A-C

84634649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 73119234-A-T

84634667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73119215-A-G

84634669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73119213-G-A

84634673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73119209-G-A

84634673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73119209-G-T

84634691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73119192-A-G

84634693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73119190-T-C

84634773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73118987-G-A

84634791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73118971-G-C

84634978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73118835-G-A

84635019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73118797-G-C

84635264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73118329-C-G

84635316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73118289-T-C

84635375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73118245-A-G

84635454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73118164-C-T

84635867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73117851-A-G

84636367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73116356-C-T

84636399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73116324-C-T

84636702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73115964-G-A

84637015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73115865-T-C

84637059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73115821-G-A

84637059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73115821-G-T

84637106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73115776-T-A

84637106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73115776-T-C

84637426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73115537-T-C

84637811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73114997-C-T

http://identifiers.org/hco/2/GRCh38#84637828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73114980-A-C

84638283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73114514-T-A

84638283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73114514-T-C

84638321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73114494-G-A

84639727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73113750-A-G

84639769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73113704-T-C

84640055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73113282-G-A

http://identifiers.org/hco/2/GRCh38#84640370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73112907-A-C

84640370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73112907-A-G

http://identifiers.org/hco/2/GRCh38#84640379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73112843-C-A

84640379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73112843-C-T

84640448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73112776-G-A

84640517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73112707-T-C

84640535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73112689-G-A

http://identifiers.org/hco/2/GRCh38#84641069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73111656-A-C

84641109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73111619-C-T

http://identifiers.org/hco/2/GRCh38#84641356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73111397-C-A

84641356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73111397-C-T

84641395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73111359-T-C

84641449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73111305-G-A

84641463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73111289-A-G

84641656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73110917-G-A

84641663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73110910-A-G

84641688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73110885-A-G

84641789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73110779-G-T

84641792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73110776-C-G

84641800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73110768-G-A

84641800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73110768-G-T

http://identifiers.org/hco/2/GRCh38#84641817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73110755-C-A

84641817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73110755-C-G

84641817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73110755-C-T

http://identifiers.org/hco/2/GRCh38#84641844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73110739-C-A

http://identifiers.org/hco/2/GRCh38#84641874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73110699-C-A

84641874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73110699-C-T

84641887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73110686-G-T

84641897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73110676-T-C

http://identifiers.org/hco/2/GRCh38#84641911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73110662-C-A

84641911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73110662-C-G

84641987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73110586-G-A

84641987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73110586-G-T

84642065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73110508-A-G

84642278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73109631-A-G

84642493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73109436-A-G

84652835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73107071-C-G

84652941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73106989-A-T

84652999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73106921-A-T

84653155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73106800-T-C

http://identifiers.org/hco/2/GRCh38#84653182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73106774-C-A

84653261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73106726-A-T

http://identifiers.org/hco/2/GRCh38#84653264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73106723-C-A

84653264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73106723-C-T

http://identifiers.org/hco/2/GRCh38#84653282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73106705-C-A

84653282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73106705-C-T

84653300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73106689-T-A

84653301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73106688-T-G

84653445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73106544-G-T

84653446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73106543-G-T

84653497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73106492-G-A

84653593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73106396-G-A

84653902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73106087-A-G

84653974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73106014-G-A

84653974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73106014-G-T

84653993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73105995-T-G

84654217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73105797-C-T

84654371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73105630-C-T

84654441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73105545-T-A

84654720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73104906-G-T

84654787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73104839-G-A

http://identifiers.org/hco/2/GRCh38#84654829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73104793-A-C

84654829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73104793-A-G

84655030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73104631-T-G

84655194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73104446-T-C

84655202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73104438-G-A

84655214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73104426-C-T

84655268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73104377-A-G

84655886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73104171-G-A

84655921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73104144-A-G

84656094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73103977-A-G

84656241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73103817-A-G

84656260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73103799-G-A

84656260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73103799-G-T

84656394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73103672-T-G

84656422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73103644-T-A

84656487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73103580-T-C

84656503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73103562-T-C

84656572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73103508-A-G

84656880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73103101-G-C

84657997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73102064-G-A

84657997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73102064-G-C

84658053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73102011-A-G

84658148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73101924-T-C

84658269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73101800-A-G

84658330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73101740-C-G

84658330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 73101740-C-T

84658361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73101709-A-G

84658479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73101591-G-A

84658506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73101348-A-G

84658536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73101318-G-T

84658654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73101209-A-G

84658882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73100990-G-T

84659149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73100751-G-A

84669251-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73099007-A-T

84669463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73098808-G-A

84669487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73098784-A-G

84669499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73098772-G-A

84669698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73098530-G-C

84670091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73097909-T-C

84670218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73097788-T-A

84670271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73097729-G-A

84670271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73097729-G-C

84670271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73097729-G-T

84670285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73097716-A-G

84670307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73097693-A-G

84670379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73097612-G-T

84670451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73097540-G-A

http://identifiers.org/hco/2/GRCh38#84670500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73097490-C-A

84670500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73097490-C-T

http://identifiers.org/hco/2/GRCh38#84670501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73097489-C-A

84670501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73097489-C-G

84670501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73097489-C-T

84670717-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73096869-T-G

84670963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73096608-G-A

84671089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73096482-C-T

84671118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73096463-G-A

84671323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73096281-T-C

84671381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73096214-C-T

84671492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73096113-A-T

84671583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73096025-T-G

84671617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73095847-A-G

http://identifiers.org/hco/2/GRCh38#84671698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73095764-C-A

84671896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73095599-T-G

http://identifiers.org/hco/2/GRCh38#84672006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73095481-C-A

84672308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73095159-A-G

84672751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73093830-G-T

84672853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73093730-G-T

84672949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73093645-T-C

84672980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73093615-C-T

84673133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73093463-G-C

84673142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73093454-C-G

84673142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73093454-C-T

84677149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73091546-T-G

84677217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73091482-T-C

84677460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73091289-G-A

84677504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73091245-G-A

84677504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73091245-G-C

84677538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73091220-G-T

84677634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73091122-C-T

84677641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73091115-A-G

84677641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73091115-A-T

84677766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73090980-C-G

84677766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73090980-C-T

84681118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73090853-G-A

http://identifiers.org/hco/2/GRCh38#84681237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73090738-A-C

http://identifiers.org/hco/2/GRCh38#84681276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73090693-C-A

84681276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73090693-C-T

84681301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73090666-A-G

http://identifiers.org/hco/2/GRCh38#84685296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73080321-C-A

84685296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73080321-C-T

http://identifiers.org/hco/2/GRCh38#84685331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73080268-C-A

84685331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 73080268-C-T

http://identifiers.org/hco/2/GRCh38#84685362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73080237-A-C

84685362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 73080237-A-G

84685449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 73080150-A-G

84685564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73080031-A-G

84685596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73079998-G-A

84685596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73079998-G-C

84685596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73079998-G-T

84685621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73079974-G-T

84686003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73079353-G-A

84686003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73079353-G-T

84686049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73079299-G-T

84686083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73079266-G-C

84686455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73078937-T-C

http://identifiers.org/hco/2/GRCh38#84686673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73078735-C-A

84686673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73078735-C-G

84686673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73078735-C-T

84686689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73078719-A-G

84688338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73077260-A-G

84688345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73077253-A-G

84688345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73077253-A-T

84688475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73077103-A-G

84688550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73077028-G-A

84688550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73077028-G-C

http://identifiers.org/hco/2/GRCh38#84688634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73076946-A-C

84688634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73076946-A-G

http://identifiers.org/hco/2/GRCh38#84688887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73076382-A-C

84688887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73076382-A-G

84689042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73076130-C-G

84689269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73075910-A-G

84689326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73075853-A-G

84689445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73075745-G-A

84689466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73075724-C-T

84689486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73075704-T-A

84689689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73075538-C-T

84689863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73075375-T-G

84690190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73074950-A-G

84693184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73073392-C-G

84693184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73073392-C-T

84693206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73073370-C-T

84693554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73073018-T-A

84693597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73072971-G-A

84693796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73072717-T-C

84693937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73072579-G-T

84693943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73072573-A-G

84694128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73072316-T-C

84694183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73072274-G-A

84694183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73072274-G-C

84694183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73072274-G-T

84694205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73072247-A-G

84694359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73072091-G-A

84694396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 73072054-T-C

84694418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73072032-A-G

84694433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73072017-G-A

84694499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73071951-C-T

84694503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73071947-G-A

84694503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73071947-G-C

84694503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73071947-G-T

84694604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73071805-T-C

84696995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73070107-T-A

84697080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73070041-G-A

84697478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73069274-A-G

84697478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73069274-A-T

84697484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73069268-T-A

84697484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73069268-T-C

84699331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73067485-A-T

84699387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73067451-G-A

84699387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73067451-G-T

84699419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73067420-T-C

84699423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73067416-G-C

84699742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 73066556-A-G

http://identifiers.org/hco/2/GRCh38#84699806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73066494-A-C

84699806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73066494-A-G

84699809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73066491-A-T

84699829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73066472-A-G

84699830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73066471-T-A

84699830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73066471-T-C

84699832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73066469-A-G

84699877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73066424-G-A

84699877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73066424-G-T

84700370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73065588-G-A

84700406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73065553-G-C

84700601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73065312-G-A

84700660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73065173-T-A

84700660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73065173-T-C

84700967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73064909-A-G

84701019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73064858-A-G

http://identifiers.org/hco/2/GRCh38#84701066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73064806-C-A

84701894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73064423-A-G

84701924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73064391-T-C

84701985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, undefined
orthologous variants: 73064340-G-C

84702077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, undefined
orthologous variants: 73064251-A-G

84702124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73064200-A-T

84702151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73064173-G-A

84702175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73064149-C-T

http://identifiers.org/hco/2/GRCh38#84703690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73062585-A-C

84703690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73062585-A-G

84703690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73062585-A-T

84703717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73062561-A-G

84703727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73062552-G-A

84703727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73062552-G-T

84703730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73062549-G-T

84703791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73062488-T-C

84703840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73062439-A-G

84703930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73062371-T-C

84704428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73061506-A-G

84704520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73061418-G-A

84705382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73060233-A-G

84705415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73060201-A-G

http://identifiers.org/hco/2/GRCh38#84705453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73060164-C-A

84705453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73060164-C-T

http://identifiers.org/hco/2/GRCh38#84705622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73059994-C-A

84705622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73059994-C-T

84705712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73059904-G-A

84705756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73059860-T-C

84705761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73059855-A-G

84705795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73059821-G-A

84705795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73059821-G-C

84705795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73059821-G-T

84705823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73059794-G-A

84705842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73059770-A-G

http://identifiers.org/hco/2/GRCh38#84705860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73059753-C-A

84705860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73059753-C-G

84706794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73053764-A-T

84706981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73053589-A-G

84707028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73053542-C-G

http://identifiers.org/hco/2/GRCh38#84707101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73053273-A-C

84707101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73053273-A-T

84707217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73053134-C-T

84707414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73052945-T-G

84707543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73052817-G-A

84707736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73052625-G-A

84707755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73052608-A-T

84707771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73052589-A-G

84707835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73052536-A-G

84707857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73052502-G-A

84707857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73052502-G-T

84707991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73052371-G-A

84708700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73052033-A-G

84708700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73052033-A-T

http://identifiers.org/hco/2/GRCh38#84709514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73051586-A-C

84709551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73051549-G-A

84709679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73051453-G-T

84710213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73050537-C-T

84710227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73050522-G-A

84710462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73050309-T-C

http://identifiers.org/hco/2/GRCh38#84710483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73050280-C-A

84710483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73050280-C-T

84710519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73050245-A-G

84710535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73050229-A-G

http://identifiers.org/hco/2/GRCh38#84710552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73050217-C-A

84710843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73049939-A-T

84711035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73049590-C-T

84711285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73049086-A-G

84711615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73048728-A-G

http://identifiers.org/hco/2/GRCh38#84711684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73048663-A-C

84711921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73048418-A-G

84712037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73048334-G-C

84712099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73048272-C-T

84712136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73048231-G-C

http://identifiers.org/hco/2/GRCh38#84712979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73047762-C-A

84712979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73047762-C-G

84712979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73047762-C-T

http://identifiers.org/hco/2/GRCh38#84712994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73047746-C-A

84712994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73047746-C-T

84713021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73047719-G-T

84713038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73047707-T-C

84713236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73047491-C-T

http://identifiers.org/hco/2/GRCh38#84713360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73047360-C-A

84713360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73047360-C-T

http://identifiers.org/hco/2/GRCh38#84713365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73047355-C-A

84713365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73047355-C-T

http://identifiers.org/hco/2/GRCh38#84713376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73047345-C-A

84713376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73047345-C-G

84713376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73047345-C-T

http://identifiers.org/hco/2/GRCh38#84713382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73047340-C-A

84713382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73047340-C-T

http://identifiers.org/hco/2/GRCh38#84713383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73047339-A-C

84713383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73047339-A-G

84713383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73047339-A-T

84715084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73046933-C-T

84715111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73046896-T-C

84715257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73046749-C-G

http://identifiers.org/hco/2/GRCh38#84715467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73046554-C-A

84715467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73046554-C-T

84715654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73046358-G-C

http://identifiers.org/hco/2/GRCh38#84718126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73044586-C-A

84718126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73044586-C-T

84718134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73044578-G-T

84718259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73044456-G-A

84718271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73044444-A-G

http://identifiers.org/hco/2/GRCh38#84718325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73044390-A-C

84718325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73044390-A-G

http://identifiers.org/hco/2/GRCh38#84718349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73044366-A-C

84718465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73043876-G-T

84718467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73043874-T-C

http://identifiers.org/hco/2/GRCh38#84718496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73043846-C-A

84718496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73043846-C-T

84718502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73043840-T-G

84718713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73043669-T-A

84718743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73043567-T-C

84718865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73043446-G-A

84719093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73043189-G-C

84719093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73043189-G-T

84719104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73043176-A-G

84722426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73042996-C-G

84722426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73042996-C-T

84722493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73042925-G-T

84722505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73042913-T-G

84722793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73042629-T-C

84722807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73042615-A-G

84722821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73042608-T-C

84722823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73042606-T-C

84722829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73042604-A-G

http://identifiers.org/hco/2/GRCh38#84722837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73042597-C-A

http://identifiers.org/hco/2/GRCh38#84722839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73042595-C-A

84722839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73042595-C-G

84723374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73042457-A-T

84723667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73041709-C-T

84723670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73041706-C-G

84723772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73041612-A-G

84723879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73041513-A-G

84725418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73039402-G-A

84725500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73039292-A-T

84725725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73038659-C-T

84725888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73038246-A-G

84726035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73037760-A-G

84727306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73037414-T-G

84727536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73037412-A-T

http://identifiers.org/hco/2/GRCh38#84727571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73037377-C-A

84727644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73037305-A-G

http://identifiers.org/hco/2/GRCh38#84733349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73030890-C-A

84733354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73030885-T-C

84733369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73030870-T-C

84733397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73030830-T-C

84733557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: synonymous variant
orthologous variants: 73030660-A-G

84733664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73030550-T-C

84733664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73030550-T-G

84733817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73030398-G-T

84733822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73030393-T-C

84742246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73029070-G-A

84742560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73028765-T-C

84742560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73028765-T-G

84742561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73028764-C-T

84742960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73028562-G-A

84743310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73028319-T-C

84743449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73028193-C-T

84743465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73028176-G-T

84743529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73028105-A-G

84743529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73028105-A-T

84743974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73027492-C-G

84744099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73027400-A-T

84744410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73027128-A-G

84744574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73026794-A-G

84744745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73026524-T-C

84744782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73026481-C-T

84744992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73026260-T-A

84744992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73026260-T-C

84745088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73026154-G-A

84745088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73026154-G-C

84745088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: stop gained
orthologous variants: 73026154-G-T

http://identifiers.org/hco/2/GRCh38#84745106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73026136-C-A

84745106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: stop gained
orthologous variants: 73026136-C-T

84745273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73025996-G-T

84745279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73025990-G-A

84745279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73025990-G-T

84745302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73025968-T-G

84745345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73025937-T-A

84745513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73025903-A-G

84745846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73025755-G-A

84745992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73025613-G-A

84746307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73025300-C-G

84746470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73024954-A-G

84746537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73024889-A-G

84750796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73023214-G-A

http://identifiers.org/hco/2/GRCh38#84750868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73023145-C-A

84750868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73023145-C-T

http://identifiers.org/hco/2/GRCh38#84750916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73023104-A-C

84750916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73023104-A-T

http://identifiers.org/hco/2/GRCh38#84750925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73023094-C-A

84750987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73023030-A-G

84750990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73023027-G-A

84751239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73022615-G-C

84751239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73022615-G-T

84751428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73022441-G-A

84751511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73022351-C-G

84751511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73022351-C-T

http://identifiers.org/hco/2/GRCh38#84762730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73021884-C-A

84762730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73021884-C-T

84762735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73021868-T-C

84762809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: stop gained
orthologous variants: 73021794-G-T

84762996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73021548-T-G

84763027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73021514-G-A

84763027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73021514-G-T

84763121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73021428-A-G

84763195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73021356-A-T

84763218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73021333-T-A

84763868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73020697-T-C

84781463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73018184-A-G

84781551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73018096-G-T

84781658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73017989-G-A

84781703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73017941-T-C

84781742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73017904-G-A

84781742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73017904-G-T

http://identifiers.org/hco/2/GRCh38#84781786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73017861-C-A

http://identifiers.org/hco/2/GRCh38#84784584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73015978-C-A

84784584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73015978-C-G

84784584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73015978-C-T

84784629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73015932-T-C

http://identifiers.org/hco/2/GRCh38#84784649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73015916-C-A

84784649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73015916-C-T

84784658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73015907-T-C

84784673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73015857-A-G

84784772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73015761-A-G

84784849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73015687-G-T

84784869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73015667-G-A

84784869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73015667-G-T

84784898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73015638-G-T

84784901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73015635-G-A

84784920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73015616-G-A

84784920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73015616-G-T

http://identifiers.org/hco/2/GRCh38#84784926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73015610-A-C

84784926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73015610-A-T

84784964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73015567-G-A

84785325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73015248-T-C

84785758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: splice donor variant
orthologous variants: 73014524-T-C

84785814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73014367-T-C

84785869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73014312-T-C

http://identifiers.org/hco/2/GRCh38#84785880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73014301-A-C

84785888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73014293-T-C

84785896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73014285-A-G

84785902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73014279-T-C

http://identifiers.org/hco/2/GRCh38#84785932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73014251-C-A

84785932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73014251-C-T

http://identifiers.org/hco/2/GRCh38#84785992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73014198-C-A

84785992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73014198-C-T

84786864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73012719-T-A

84786864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73012719-T-C

84786897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73012693-T-C

84787047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73012549-G-T

84787108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73012462-A-G

http://identifiers.org/hco/2/GRCh38#84787138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73012433-C-A

84787138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73012433-C-T

84787227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73012344-G-A

84787227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: stop gained
orthologous variants: 73012344-G-T

http://identifiers.org/hco/2/GRCh38#84787334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73012237-C-A

http://identifiers.org/hco/2/GRCh38#84787342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73012231-C-A

84787342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73012231-C-G

84787342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73012231-C-T

84787356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73012217-T-C

84787457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73012119-A-G

84795850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73011217-C-G

84796215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73010710-G-A

84796484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73010467-T-C

http://identifiers.org/hco/2/GRCh38#84796542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73010443-C-A

84796542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73010443-C-T

http://identifiers.org/hco/2/GRCh38#84796544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73010441-C-A

84796544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73010441-C-T

http://identifiers.org/hco/2/GRCh38#84796652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73010357-A-C

84796925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73010269-A-G

84796926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73010268-G-A

84796952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73010242-A-G

84797230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73009963-A-G

84797254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73009938-G-A

84797266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73009926-A-G

84797768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73009419-A-T

http://identifiers.org/hco/2/GRCh38#84805530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73004640-C-A

84805530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73004640-C-T

84805560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73004621-T-C

84805594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73004586-A-G

84805601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73004579-G-A

84805601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73004579-G-T

84805614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73004565-G-T

84805617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73004562-T-A

84805628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73004556-T-C

84805647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73004538-C-T

84805725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73004460-G-A

84805916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73004264-C-G

84805936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73004242-A-G

84805946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73004233-T-G

84806006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73004173-C-T

84806067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73004125-G-A

84806067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73004125-G-T

http://identifiers.org/hco/2/GRCh38#84807629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73003776-A-C

84807664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73003730-T-C

84807692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73003703-C-T

84807865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73003443-C-T

84807879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73003429-C-T

84808269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73003046-A-G

http://identifiers.org/hco/2/GRCh38#84808513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73002725-C-A

84808513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73002725-C-G

84808513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73002725-C-T

http://identifiers.org/hco/2/GRCh38#84808540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73002698-C-A

84808566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73002672-T-C

84808615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73002618-T-C

http://identifiers.org/hco/2/GRCh38#84808616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73002617-C-A

84812458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 73001874-G-A

84812514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: synonymous variant
orthologous variants: 73001818-C-T

84812548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73001782-G-A

84812548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73001782-G-C

84812566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73001764-G-A

84812567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73001763-G-A

84812567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73001763-G-T

84812584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73001746-T-C

84812726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73001614-T-C

84812746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73001593-T-C

84812787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73001554-G-T

84812788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73001553-G-A

84812930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73001428-G-T

84812941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73001417-A-G

84812958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73001400-G-T

http://identifiers.org/hco/2/GRCh38#84812984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73001383-C-A

84812984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73001383-C-T

84813137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 73001228-G-A

84813196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73001183-G-A

84813196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73001183-G-T

84813270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73001117-T-A

84813270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73001117-T-C

http://identifiers.org/hco/2/GRCh38#84813278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#73001109-C-A

84813504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73000680-G-T

84813631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 73000564-T-C

84813776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 72999874-G-T

84813860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 72999567-G-T

http://identifiers.org/hco/2/GRCh38#84813888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72999540-C-A

84813897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 72999531-T-A

84813907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 72999521-G-A

84813907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 72999521-G-T

84813933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 72999505-G-A

84813973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 72999469-A-G

84814134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 72999308-C-G

84814230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 72999222-G-A

84814230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 72999222-G-T

http://identifiers.org/hco/2/GRCh38#84814269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72999185-C-A

84814269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 72999185-C-G

84814269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 72999185-C-T

84814358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 72999095-G-A

84814358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 72999095-G-T

84814417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 72999042-G-A

84814473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 72998982-G-T

84816023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 72998148-A-G

84816038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 72998133-C-G

84816038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: missense variant
orthologous variants: 72998133-C-T

84816089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 72998082-G-T

84816798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 72997636-C-G

84816815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 72997619-A-T

84819179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 72995020-T-C

84819179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 72995020-T-G

84819293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 72994838-A-G

84819293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: intron variant
orthologous variants: 72994838-A-T

http://identifiers.org/hco/2/GRCh38#84819438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72994710-C-A

84819530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: 3 prime UTR variant
orthologous variants: 72994647-T-G

http://identifiers.org/hco/2/GRCh38#84819546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72994631-C-A

84819546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: 3 prime UTR variant
orthologous variants: 72994631-C-G

84819546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: 3 prime UTR variant
orthologous variants: 72994631-C-T

84819551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: 3 prime UTR variant
orthologous variants: 72994626-G-T

84819589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2951
most severe consequence: 3 prime UTR variant
orthologous variants: 72994587-A-T