80628695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9492322-C-T

80629065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9492677-G-A

80629065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9492677-G-T

80629272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9492882-A-G

80629346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9492955-A-G

80629858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9493469-T-C

http://identifiers.org/hco/8/GRCh38#80630366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9494011-C-A

80630567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9494204-T-C

http://identifiers.org/hco/8/GRCh38#80630624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9494255-C-A

80630838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9494471-A-G

80630993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9494595-C-T

80631337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9494863-G-A

80631458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9494969-A-G

http://identifiers.org/hco/8/GRCh38#80631533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9495026-C-A

80631540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495033-T-C

http://identifiers.org/hco/8/GRCh38#80631596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9495075-C-A

80631652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495101-C-T

80631670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495119-G-T

80631724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495143-G-A

80631724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495143-G-T

http://identifiers.org/hco/8/GRCh38#80631794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9495219-A-C

80631794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495219-A-G

80631897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495319-T-C

80631994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495404-G-A

80631994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495404-G-T

80632009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495412-G-A

80632009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495412-G-T

http://identifiers.org/hco/8/GRCh38#80632019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9495422-C-A

80632019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495422-C-T

80632063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495445-T-A

80632098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495495-G-C

80632222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495613-G-T

80632228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495619-T-C

80632280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495663-C-T

80632285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495668-A-G

80632310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495692-C-T

http://identifiers.org/hco/8/GRCh38#80632313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9495695-C-A

80632320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495702-C-T

80632325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495707-A-G

http://identifiers.org/hco/8/GRCh38#80632379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9495750-C-A

80632627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495885-T-C

80632648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495896-G-C

80632735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9495977-T-A

http://identifiers.org/hco/8/GRCh38#80632787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9496019-C-A

80632830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9496071-G-A

80632982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9496168-G-C

80632982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9496168-G-T

80633032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9496215-A-G

80633125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9496303-G-T

80633355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9496524-T-C

80633422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9496554-G-A

80633422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9496554-G-T

80633462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9496589-G-A

80633521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9496619-G-T

80633530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9496627-T-C

80633558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9496652-G-T

80633613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9496684-G-A

80633613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9496684-G-T

http://identifiers.org/hco/8/GRCh38#80633631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9496702-C-A

80633631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9496702-C-G

80633915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9496986-T-C

80634080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9497147-A-T

http://identifiers.org/hco/8/GRCh38#80634094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9497160-C-A

80634094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9497160-C-G

http://identifiers.org/hco/8/GRCh38#80634119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9497184-C-A

80634119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9497184-C-T

80634152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9497216-T-C

http://identifiers.org/hco/8/GRCh38#80634202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9497345-C-A

80634202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9497345-C-T

http://identifiers.org/hco/8/GRCh38#80634240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9497379-C-A

http://identifiers.org/hco/8/GRCh38#80634385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9497562-C-A

80634385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9497562-C-T

80634390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9497567-A-G

80634419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9497596-T-C

80634582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9497750-T-C

http://identifiers.org/hco/8/GRCh38#80634736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9497864-C-A

80634787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9497915-G-A

80634787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9497915-G-C

80634787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9497915-G-T

80634864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9497995-T-G

80634893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9498028-G-T

80635018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9498157-C-T

80635023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9498162-T-C

80635023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9498162-T-G

80635056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9498204-T-A

80635062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9498209-G-A

80635175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9498317-G-C

http://identifiers.org/hco/8/GRCh38#80635336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9498448-A-C

80635443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9498494-T-A

80635952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9498981-T-A

80636143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9499167-A-G

80636330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9499349-A-G

80636352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9499371-T-C

80636490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9499499-T-C

80636492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9499501-C-T

http://identifiers.org/hco/8/GRCh38#80636562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9499566-C-A

80636562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9499566-C-T

http://identifiers.org/hco/8/GRCh38#80636566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9499570-A-C

http://identifiers.org/hco/8/GRCh38#80636659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9499663-C-A

80636659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9499663-C-T

80636662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9499666-G-A

80636898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9499887-A-G

80636913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9499902-C-T

80637103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9500059-A-G

http://identifiers.org/hco/8/GRCh38#80637121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9500077-A-C

80637181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9500134-T-A

http://identifiers.org/hco/8/GRCh38#80637182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9500135-A-C

80637299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9500251-T-C

http://identifiers.org/hco/8/GRCh38#80637505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9500466-C-A

80637631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9500587-G-C

80637636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9500592-G-T

80637836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9500768-T-C

80637891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9500801-T-C

80637891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9500801-T-G

80638039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9500883-G-T

http://identifiers.org/hco/8/GRCh38#80638075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9500919-C-A

80638075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9500919-C-T

80638115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9500958-G-T

80638119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9500962-G-A

80638119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9500962-G-T

80638253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9501090-T-C

80638257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9501094-A-G

80638348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9501147-G-T

http://identifiers.org/hco/8/GRCh38#80638374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9501172-C-A

80638744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9501473-T-C

80638801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9501532-A-G

80638900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9501633-A-G

http://identifiers.org/hco/8/GRCh38#80639075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9501765-C-A

80639075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9501765-C-T

80639107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9501797-A-G

http://identifiers.org/hco/8/GRCh38#80639140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9501838-C-A

80639471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9502121-T-C

80639680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9502325-G-C

80639872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9502511-T-C

80639893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9502529-T-C

80639966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9502583-T-A

80639967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9502584-A-G

80640053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9502657-T-C

http://identifiers.org/hco/8/GRCh38#80640228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9502828-C-A

http://identifiers.org/hco/8/GRCh38#80640235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9502835-C-A

80640235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9502835-C-T

80640236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9502836-G-C

80640247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9502847-A-G

80640266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9502862-T-C

80640276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9502872-A-G

80640330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9502911-G-A

80640330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9502911-G-C

80640333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9502914-G-A

http://identifiers.org/hco/8/GRCh38#80640411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9502970-C-A

http://identifiers.org/hco/8/GRCh38#80640476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9503035-C-A

80640500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9503059-T-C

80640523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9503082-T-C

80640696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9503234-G-T

80641019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9503557-A-G

80641127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9503663-A-G

80641145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9503676-G-A

80641145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9503676-G-T

http://identifiers.org/hco/8/GRCh38#80641227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9503734-A-C

80641227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9503734-A-T

80641255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9503746-T-C

80641511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9503994-G-C

80641511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9503994-G-T

80641523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9504005-G-A

80641523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9504005-G-C

80641523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9504005-G-T

80641552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9504022-T-A

80641552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9504022-T-C

80641552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9504022-T-G

80641562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9504033-G-A

80641562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9504033-G-C

80641562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9504033-G-T

http://identifiers.org/hco/8/GRCh38#80641570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9504041-A-C

80641570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9504041-A-G

80641570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9504041-A-T

http://identifiers.org/hco/8/GRCh38#80641573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9504044-A-C

80641573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9504044-A-G

80642898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9504712-T-A

80642898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9504712-T-C

80642915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9504729-G-A

80643106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 9504916-C-T

80656002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9506397-G-T

80656165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9506573-C-T

80656183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9506586-A-G

80656201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9506604-T-C

80656219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9506641-T-C

80656220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9506642-G-A

80656281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9506705-G-A

80656531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9506802-C-T

80656552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9506823-T-C

80656554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9506825-A-G

http://identifiers.org/hco/8/GRCh38#80656574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9506850-A-C

80656645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9506912-C-T

80657746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9507737-C-T

80657923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9507837-G-A

80657984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9507900-T-C

http://identifiers.org/hco/8/GRCh38#80657992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9507908-C-A

80658005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9507921-C-T

80658424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9509592-A-T

http://identifiers.org/hco/8/GRCh38#80658519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9509659-C-A

80658519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9509659-C-T

http://identifiers.org/hco/8/GRCh38#80658544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9509684-C-A

80658646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9509775-G-T

80658702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9509828-T-C

80658757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9509874-A-G

http://identifiers.org/hco/8/GRCh38#80658758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9509875-C-A

80658769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9509886-A-G

80659085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9510142-T-C

80659204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9510265-C-T

80659570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9511011-C-T

80659730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9511165-T-A

80659730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9511165-T-C

80659730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9511165-T-G

80659881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9511297-C-T

80660098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9511466-C-T

80664680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9512231-G-T

80664700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9512251-G-A

80664700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9512251-G-T

80664771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9512313-G-T

80664959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 9512479-G-A

80665010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 9512530-G-A

80665091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9512610-A-G

http://identifiers.org/hco/8/GRCh38#80665146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9512661-C-A

http://identifiers.org/hco/8/GRCh38#80665152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9512667-C-A

80665172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9512684-T-C

80665173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9512685-G-A

80665173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9512685-G-C

80665173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9512685-G-T

http://identifiers.org/hco/8/GRCh38#80665174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9512686-C-A

80665191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9512699-T-C

80665213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9512720-T-C

80670613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9517436-G-A

80670613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9517436-G-C

80670613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9517436-G-T

80670623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9517446-A-G

80670626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9517449-T-A

80679222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9526600-A-G

80679236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9526614-T-C

80679408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9526771-C-T

http://identifiers.org/hco/8/GRCh38#80679696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9527048-C-A

http://identifiers.org/hco/8/GRCh38#80679714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9527057-A-C

http://identifiers.org/hco/8/GRCh38#80682567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9531221-C-A

80682596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9531250-T-C

80682597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9531251-G-A

80683025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9531477-C-G

80683129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9531579-T-C

80683129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9531579-T-G

http://identifiers.org/hco/8/GRCh38#80683270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9532428-C-A

80683322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9532471-C-T

80683456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9532523-T-C

80683505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9532549-C-T

80683600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9532631-A-G

80683653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9532680-T-A

80683686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9532713-G-A

80683810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9532803-G-A

80683829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9532822-C-G

80683833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9532826-T-C

80683838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9532831-A-G

80683892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9532857-G-T

80683962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9532888-G-A

80683997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9532922-T-A

80684452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9533294-A-G

80684547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9533389-G-A

80684688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9533876-T-A

80684833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9534016-A-G

80685179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9534428-G-A

80685179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9534428-G-C

80685227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9534480-G-A

80685275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9534528-G-A

80685370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9534629-T-C

80685790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9534920-A-G

80685814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9534944-G-T

80685917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9535006-T-C

80686799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9535656-G-A

80686921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9535727-C-G

80687037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9535837-T-C

80687086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9535874-A-G

80687090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9535878-T-C

http://identifiers.org/hco/8/GRCh38#80687207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#9535941-C-A

80687207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9535941-C-T

80687219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 9535945-C-T

http://identifiers.org/hco/8/GRCh38#80687223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#9535949-A-C

80687298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 9536024-C-T

http://identifiers.org/hco/8/GRCh38#80687301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#9536027-C-A

80687301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 9536027-C-T

http://identifiers.org/hco/8/GRCh38#80687334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#9536060-C-A

80687334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 9536060-C-G

80687334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 9536060-C-T

http://identifiers.org/hco/8/GRCh38#80687352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9536078-C-A

80687352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 9536078-C-T

80687364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 9536090-G-A

80687394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 9536120-G-T

http://identifiers.org/hco/8/GRCh38#80687436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#9536156-C-A

80687436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 9536156-C-T

80687448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 9536168-G-A

80687448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9536168-G-T

80687521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9536215-G-A

80687521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9536215-G-T

80687526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9536218-G-T

80687567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9536249-T-C

http://identifiers.org/hco/8/GRCh38#80689065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9537153-C-A

http://identifiers.org/hco/8/GRCh38#80689144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9537236-A-C

80689145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9537237-C-T

http://identifiers.org/hco/8/GRCh38#80689248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9537334-A-C

80689329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9537419-T-G

80689682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9537690-C-T

80689730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9537735-G-A

http://identifiers.org/hco/8/GRCh38#80689778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9537771-C-A

80689819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9537775-T-C

80689822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9537778-T-C

80689956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9537879-A-G

80690024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9537950-T-C

80690219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9538305-C-G

http://identifiers.org/hco/8/GRCh38#80690391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9538462-C-A

80690422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9538491-C-T

80692162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9538774-C-T

80692234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9538834-T-C

80692267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9538870-G-C

80692309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9538919-T-C

80692313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9538923-C-G

80692313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9538923-C-T

80692363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9538974-C-T

80692402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9538999-T-C

80692535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539127-G-T

http://identifiers.org/hco/8/GRCh38#80692711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9539294-A-C

80692775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539363-A-G

80692903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539470-G-A

80692903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539470-G-T

80692995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539550-T-C

80693059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 9539614-T-C

http://identifiers.org/hco/8/GRCh38#80693177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9539700-C-A

80693177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539700-C-T

80693181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539704-G-C

80693181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539704-G-T

80693189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539707-T-C

80693189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539707-T-G

80693213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539730-G-A

80693213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539730-G-T

80693219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539736-C-T

80693244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539759-T-C

80693320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539818-T-C

80693393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539887-T-C

80693525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539959-G-A

80694706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9540158-G-A

http://identifiers.org/hco/8/GRCh38#80694844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9540285-C-A

http://identifiers.org/hco/8/GRCh38#80695053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9540452-C-A

80695556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9541108-T-C

http://identifiers.org/hco/8/GRCh38#80695855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9542711-C-A

80695855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9542711-C-T

80696006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9542845-T-C

http://identifiers.org/hco/8/GRCh38#80696037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9542875-C-A

80696185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9543020-T-C

80696186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9543021-G-A

80698971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9543252-G-A

80699038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9543319-A-G

80699181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9543465-G-C

80699274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9543586-A-G

80703991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9545831-C-T

80704036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9545892-T-C

http://identifiers.org/hco/8/GRCh38#80704166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9545997-C-A

80704166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9545997-C-T

80705279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9546291-G-A

80705279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9546291-G-C

80705307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9546328-C-G

http://identifiers.org/hco/8/GRCh38#80706129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9546766-A-C

80706163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9546792-G-C

80706475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9547105-A-G

80706869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9547603-A-G

80707074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9547756-G-A

80707079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9547766-G-T

80707843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9550217-A-G

80707862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9550230-G-A

80708268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9550558-T-C

80708401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9550692-A-G

80708430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9550721-T-G

80708549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9550841-T-C

80708669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9550957-G-A

80708765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9551051-T-C

80708815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9551101-C-T

80708914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9551168-G-A

80709003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9551244-T-C

80709016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9551256-G-A

80709089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9551326-T-C

80709098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9551335-A-T

80709115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9551351-A-G

80710402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9553503-C-T

80710663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9553715-C-T

80711014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9553994-G-A

http://identifiers.org/hco/8/GRCh38#80711311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9554322-C-A

http://identifiers.org/hco/8/GRCh38#80713256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9556340-A-C

80713387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9556473-G-A

80713453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9556496-C-T

http://identifiers.org/hco/8/GRCh38#80713498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9556541-C-A

80713498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9556541-C-G

80713498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9556541-C-T

80713550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9556592-T-C

80713843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9556869-T-C

http://identifiers.org/hco/8/GRCh38#80713859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9556885-A-C

http://identifiers.org/hco/8/GRCh38#80713979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9557531-A-C

80714027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9557578-T-G

80714099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9557682-G-A

80714144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9557726-A-T

80714296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9557845-A-G

http://identifiers.org/hco/8/GRCh38#80714474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9558144-C-A

80714498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9558162-A-G

80714630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9558275-G-T

80714683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9558330-G-C

80714889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9558516-C-T

80715168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9558822-C-T

80716151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9559888-A-G

80716313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9560068-T-G

80716363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9560114-C-T

80716494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9560218-G-A

80716606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9560329-T-G

80716638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9560360-T-C

80716644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9560366-T-G

80716774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9560493-G-C

80716835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9560545-G-A

80716925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9560628-C-T

80717064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9560773-T-C

80717107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9560818-G-A

80717158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9560853-T-C

http://identifiers.org/hco/8/GRCh38#80717375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9561045-A-C

80717387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9561056-G-T

80717549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9561208-T-G

80717815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9561421-T-C

80717861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9561465-T-C

80718162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9561680-G-A

80718271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9561773-C-T

80718480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9561941-G-C

80718489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9561950-A-G

80718534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9562003-G-A

80718600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9562061-G-A

80718876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9562331-T-C

80719340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9562490-T-C

80719401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9562545-T-C

80719611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9562743-T-A

http://identifiers.org/hco/8/GRCh38#80719669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9562799-A-C

80719669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9562799-A-G

80719735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9562864-G-A

http://identifiers.org/hco/8/GRCh38#80719831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9562922-A-C

80719889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9562982-T-C

80719990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9563078-G-A

http://identifiers.org/hco/8/GRCh38#80725561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9563412-A-C

80725635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9563492-A-T

80725729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9563573-C-T

80725734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9563578-C-T

80725792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9563636-G-A

80725902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9563731-G-T

http://identifiers.org/hco/8/GRCh38#80726020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9563837-A-C

80726285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9564072-A-T

80726708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9564776-T-A

80726880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565006-G-A

http://identifiers.org/hco/8/GRCh38#80727003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9565140-C-A

80727040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565178-G-A

80727151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565255-G-T

80727165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565272-C-G

80727201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565303-T-C

80727327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565425-G-A

80727606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565865-G-A

80727606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565865-G-T

80728043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9566238-C-T

80728053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9566248-T-C

80728813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9568612-C-T

80729155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9568899-A-G

80729370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9568972-A-G

80729469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9569048-A-T

80729478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9569057-G-A

80729535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9569111-T-A

80729612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9569175-T-C

80729637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9569198-T-C

80729700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9569261-C-T

80729990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9570215-C-T

80730159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9570365-T-G

80730194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9570398-A-T

80730236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9570442-T-C

80730933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9570738-C-T

80733561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9573208-G-A

80733591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9573241-C-T

80734064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9573796-T-C

http://identifiers.org/hco/8/GRCh38#80734146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9573880-C-A

80734146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9573880-C-G

80734483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9574205-A-G

80734502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9574224-A-G

80734797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9574754-T-A

http://identifiers.org/hco/8/GRCh38#80735164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9575044-A-C

80735164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9575044-A-G

80735182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9575062-C-T

80735194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9575083-G-A

http://identifiers.org/hco/8/GRCh38#80735261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9575138-A-C

80744069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9578446-G-A

80744469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9578903-T-C

80744704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9579129-C-T

80745151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9579668-A-G

80745335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9580028-T-G

80745508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9580193-T-C

80745667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9580348-T-G

80745781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9580454-T-G

80745877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9580505-A-T

80745884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9580512-T-C

80745949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9580569-C-T

80746096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9580699-C-T

80746374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9581201-T-A

80746563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9581386-G-A

80746600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9581423-T-C

http://identifiers.org/hco/8/GRCh38#80746604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9581427-C-A

80746604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9581427-C-G

80746861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9581626-T-A

80746861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9581626-T-C

80746861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9581626-T-G

80747037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9581796-T-C

80747269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9582028-G-A

80747298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9582057-A-T

80747304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9582063-T-C

80747311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9582074-T-C

80748533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9583050-A-G

80748616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9583125-G-A

80752084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9584776-A-T

80752119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9584810-T-G

80752122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9584813-T-G

80752130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9584821-A-G

http://identifiers.org/hco/8/GRCh38#80752228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#9584920-A-C

80752230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9584922-T-G

80752423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9585109-A-G

80752474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9585160-T-C

http://identifiers.org/hco/8/GRCh38#80752839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9585207-C-A

80753083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9585429-A-G

80753084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9585430-T-C

80753213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9585553-G-C

80753217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9585557-G-A

http://identifiers.org/hco/8/GRCh38#80753233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#9585573-C-A

80753284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9585612-G-A

80753319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9585636-G-A

80753537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9585868-T-C

80753579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9585910-G-A

80753595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9585925-G-T

80753653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9585975-A-G

80753729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9586185-T-C

80754033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9586436-G-C

80754033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9586436-G-T

80754079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9586485-A-G

80755521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9587724-A-G

80756579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9588431-T-A

80756583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9588435-A-G

80756944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9588724-G-A

80758130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9588895-C-T

80758195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9588966-C-T

http://identifiers.org/hco/8/GRCh38#80758396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9589160-C-A

80758535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9589293-G-A

80758627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9589419-T-C

http://identifiers.org/hco/8/GRCh38#80758715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9589514-C-A

http://identifiers.org/hco/8/GRCh38#80758716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9589515-A-C

80758736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9589531-T-C

http://identifiers.org/hco/8/GRCh38#80759077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9589760-C-A

80767075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9590726-A-G

80767136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9590787-C-T

80767728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9591372-C-T

80767779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9591395-C-T

80767789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9591405-T-G

80767827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9591440-A-G

80767881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9591493-A-G

80768395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9591938-G-A

80768480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9591987-G-A

80768490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9591997-T-C

http://identifiers.org/hco/8/GRCh38#80768586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9592093-C-A

80768604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9592111-A-G

80768654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9592169-G-A

http://identifiers.org/hco/8/GRCh38#80768755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9592264-C-A

80768755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9592264-C-T

80768787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9592276-A-G

80768841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9592311-C-G

80773263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9593812-C-T

80773455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9593972-T-C

80773684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9594202-A-G

80773958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9594449-T-C

80774361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9595102-C-T

80774426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9595205-G-A

80774499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9595296-T-A

80774499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9595296-T-C

80774503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9595300-C-T

80774525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9595306-G-T

80774607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9595362-C-T

80774726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9595452-G-A

http://identifiers.org/hco/8/GRCh38#80774905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9595589-C-A

80774905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9595589-C-T

80775091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9595771-G-A

80775169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9595900-C-T

80775221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9595952-T-C

80775283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9596009-T-C

http://identifiers.org/hco/8/GRCh38#80775476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9596183-A-C

80775695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9596369-G-A

80775720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9596396-T-C

80775841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9596491-A-G

http://identifiers.org/hco/8/GRCh38#80775861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9596510-A-C

80779968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9603074-T-A

80780042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9603147-G-A

80780055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9603161-G-A

80780158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9603261-G-A

80780195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9603284-G-A

80780351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9603430-T-G

80780405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9603486-T-C

80780711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9603695-G-A

80780713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9603697-G-A

80780869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9603816-T-A

80780960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9603878-T-C

80781083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9603995-A-T

80785994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9606934-A-G

80785994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9606934-A-T

80785998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9606938-A-G

80786017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9606956-T-C

80786106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9607065-C-T

80786310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9607302-T-C

80786310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9607302-T-G

http://identifiers.org/hco/8/GRCh38#80786317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9607308-A-C

80786516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9607471-T-G

80786652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9607541-A-G

80786716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9607609-G-A

80786727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9607620-A-G

80787010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9607864-G-C

80787037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9607890-T-A

80791869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9609914-T-C

80791936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9609976-G-A

80792021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9610039-T-C

80792221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9610179-C-T

80792274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9610224-T-C

80792415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9610288-G-T

80792461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9610333-A-G

80792834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9610657-C-T

80792889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9610720-A-G

80792936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9610767-A-G

80793482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9611099-T-A

80793482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9611099-T-G

80793898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9611501-A-G

80793939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9611568-T-G

80794166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9611728-G-A

80794179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9611737-T-A

80794179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9611737-T-C

80794579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9612050-A-G

80794585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9612056-C-T

80794644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9612115-T-C

80794664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9612128-G-C

80794716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9612176-A-G

http://identifiers.org/hco/8/GRCh38#80794896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9612318-C-A

80794896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9612318-C-G

http://identifiers.org/hco/8/GRCh38#80794936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9612374-C-A

80794939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9612377-A-G

80795104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9612512-C-T

80795168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9612555-G-A

80795172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9612559-C-T

http://identifiers.org/hco/8/GRCh38#80795173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9612560-A-C

http://identifiers.org/hco/8/GRCh38#80795284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9612658-A-C

80795438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9612811-T-G

80795475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9612846-T-C

80795475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9612846-T-G

http://identifiers.org/hco/8/GRCh38#80795477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9612848-A-C

80795533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9612898-A-G

80795544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9612909-T-C

80795545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9612910-T-C

80795948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9613159-G-A

80805711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9614820-C-T

80805723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9614833-T-A

80805723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9614833-T-C

http://identifiers.org/hco/8/GRCh38#80805864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#9614967-A-C

80806240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9615273-A-T

80806368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9615397-C-T

http://identifiers.org/hco/8/GRCh38#80806396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9615430-C-A

80806481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9615506-T-C

80806813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9615795-C-T

80806936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9615883-G-A

80807026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9615965-G-A

80807083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9616014-T-C

80807086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9616015-T-C

80807117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9616043-T-G

80807428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9616398-T-A

80807553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9616504-C-T

80807587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9616530-A-G

80807710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9616597-T-A

80807852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9616731-A-G

80808087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9617282-T-C

80808088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9617283-G-A

80808240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9617433-A-G

80808241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9617434-T-C

80808342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9617512-T-C

80808586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9618126-G-A

80808605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9618144-G-T

80808770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9618342-T-C

80808810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9618386-T-A

80808921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9618482-T-C

80808994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9618538-A-G

80809167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9618554-T-G

80809370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9618599-T-A

80809418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9618649-G-T

80809451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9618682-G-T

80809564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9618801-T-C

80809613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9618849-C-T

80809642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9618878-G-A

80809752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9619000-T-C

http://identifiers.org/hco/8/GRCh38#80809878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9619149-C-A

80810122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9619335-T-A

80810197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9619391-G-A

http://identifiers.org/hco/8/GRCh38#80810228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#9619419-C-A

80810228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9619419-C-T

80810488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9619682-A-T

80810536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9619726-T-C

http://identifiers.org/hco/8/GRCh38#80810617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9619789-A-C

80810674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9619848-G-A

80810706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9619878-A-G

80811055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9620143-T-C

80811080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9620168-A-G

80811211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9620271-T-A

80811212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9620272-G-A

80814053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9621533-T-C

80814167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9621629-T-C

80814457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9621929-T-C

80814742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9622193-T-G

80815231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9623239-C-T

80815317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9623324-T-C

http://identifiers.org/hco/8/GRCh38#80815417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9623428-A-C

80815789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9623978-T-C

http://identifiers.org/hco/8/GRCh38#80815850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9624040-C-A

80816054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9624344-G-A

80816064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9624355-C-T

http://identifiers.org/hco/8/GRCh38#80817854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9626626-C-A

80818092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9626852-A-G

80818102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9626861-C-T

80818216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9626931-T-A

80818233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9626948-G-T

80818248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9626963-G-A

80818320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9627040-A-G

80818928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9627374-T-C

80818928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9627374-T-G

80818965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9627406-T-C

http://identifiers.org/hco/8/GRCh38#80818979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9627420-A-C

http://identifiers.org/hco/8/GRCh38#80819267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9627701-A-C

80819267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9627701-A-T

80819487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9628109-T-A

http://identifiers.org/hco/8/GRCh38#80819512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9628134-C-A

http://identifiers.org/hco/8/GRCh38#80819541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9628156-C-A

http://identifiers.org/hco/8/GRCh38#80819595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9628208-A-C

80819601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9628214-G-A

80819646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9628260-A-G

80819647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9628261-T-C

80819842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9628451-T-G

80819882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9628494-G-C

80819995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9628605-T-A

80820237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9628824-G-A

80820528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9629160-T-C

80820624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9629270-G-T

80821143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9629939-A-G

80821286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9630057-T-C

80821286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9630057-T-G

80821315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9630079-A-G

http://identifiers.org/hco/8/GRCh38#80821319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9630083-A-C

80821319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9630083-A-G

80821363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9630113-T-C

80821531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9630275-G-T

80821538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 9630282-A-G

80821720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9630438-A-G

http://identifiers.org/hco/8/GRCh38#80821814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9630534-C-A

80821823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9630543-A-G

80829032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9631341-C-T

80829274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9631511-T-C

80829279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9631516-T-C

80829304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9631546-G-C

80829307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9631549-G-A

http://identifiers.org/hco/8/GRCh38#80829346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9631586-C-A

http://identifiers.org/hco/8/GRCh38#80829378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9631612-C-A

80829669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9631885-T-C

80829788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9631991-A-G

80829900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9632099-A-G

80831216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9632611-C-T

80831412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9632787-G-A

http://identifiers.org/hco/8/GRCh38#80832371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9637404-C-A

80832371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9637404-C-T

80832374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9637407-C-G

80832374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9637407-C-T

80832471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9637465-C-T

80832475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9637469-C-T

80832672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9637650-A-G

80832701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9637672-A-T

80832789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9637756-C-T

80832817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9637783-C-T

80832818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9637784-C-T

80832950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9637913-T-C

80833517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9638571-C-T

80833550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9638606-T-C

80833593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9638646-G-A

80836960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9640266-C-T

80836980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9640285-C-T

80837164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9640461-T-C

80837178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9640475-G-A

80837571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9640810-G-C

80837674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9640919-A-G

80837682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9640927-A-G

80837816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9641058-C-T

80838234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9641356-C-T

80838238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9641360-A-G

80838282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9641406-T-C

80838304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9641417-G-A

http://identifiers.org/hco/8/GRCh38#80839352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9642800-C-A

http://identifiers.org/hco/8/GRCh38#80839568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9643012-C-A

80839580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9643024-G-A

80839589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9643033-T-C

80839716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9643146-C-T

80839730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9643160-G-A

80839991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9643532-T-C

80840084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9643618-T-C

80840634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9644051-G-A

80840658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9644075-G-A

80840662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9644079-T-C

http://identifiers.org/hco/8/GRCh38#80840748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9644153-C-A

80840748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9644153-C-G

http://identifiers.org/hco/8/GRCh38#80841172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9644536-A-C

80841220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9644584-T-C

80841343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9644716-G-A

80841718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9645038-T-C

80841761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9645081-T-A

80842220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9645198-A-G

80843254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9646607-C-T

80843810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9647338-A-G

80843858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9647385-C-T

80843915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9647439-G-A

80845199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9649408-C-G

80845262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9649463-C-T

80845316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9649516-C-T

80845475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9649666-C-G

80845532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9649705-A-G

80845551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9649724-G-T

80845736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9649865-C-T

80845844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9649955-T-C

80845961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9650061-T-A

80846050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9650129-A-T

80846090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9650229-G-A

80846098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9650237-G-C

80852906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9653765-G-C

80852957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9653810-C-T

http://identifiers.org/hco/8/GRCh38#80853572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9654098-C-A

80853572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9654098-C-T

80853697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9654181-C-T

80853770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9654235-T-G

80853903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9654322-G-A

80853903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9654322-G-C

80860045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9656486-T-C

80860055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9656496-G-A

80860084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9656518-G-C

80860088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9656522-T-C

80860753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9657513-G-A

80860791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9657551-T-C

http://identifiers.org/hco/8/GRCh38#80860900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9657639-A-C

80861458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9658231-G-A

80863080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9659449-T-C

80863089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9659458-A-G

80863322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9659729-G-A

80863642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9660032-G-C

80863662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9660034-T-C

80863902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9660210-C-T

80863939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9660246-C-T

80864299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9661884-C-T

http://identifiers.org/hco/8/GRCh38#80864402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9662008-C-A

80864691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9662296-T-C

http://identifiers.org/hco/8/GRCh38#80865044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#9662903-C-A

80865044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9662903-C-T

80865254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9663080-C-T

80865255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9663081-G-A

80865255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9663081-G-C

80865255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9663081-G-T

80865520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9663441-T-A

80865520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9663441-T-G

80866330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9664614-C-T

80866342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9664625-T-A

80866574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9664834-C-T

80866730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9664965-G-C

80866787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9665012-G-A

80866787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9665012-G-C

80866798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9665023-T-C

80866913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9665030-C-G

80866913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9665030-C-T

80866948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9665067-T-C

80867265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9665331-C-T

80867446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9665498-G-A

80867446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9665498-G-T

80867545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9665577-T-C

80867837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9665860-T-C

80867859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9665884-T-C

80867950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9665976-C-T

http://identifiers.org/hco/8/GRCh38#80868043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9666074-C-A

80868086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9666117-T-C

80868717-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9668959-T-G

80868745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9668972-T-C

80868846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9669056-G-A

80868864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9669080-G-A

80868864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9669080-G-C

80869162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9669337-G-A

80869212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9669389-A-G

80869225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9669402-T-C

80869348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9669523-T-A

80869351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9669526-A-G

80869374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9669586-C-T

80869399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9669610-A-G

80869425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9669628-T-C

80869596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9669789-A-G

80869610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9669806-G-T

80869637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9669833-G-C

80869675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9669877-C-T

80869698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9669902-T-G

http://identifiers.org/hco/8/GRCh38#80869778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9669983-C-A

80869797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9670004-G-A

80870018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9670139-A-G

80870041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9670160-T-C

80870042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9670161-T-C

80870049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9670168-T-C

80870074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9670192-A-G

http://identifiers.org/hco/8/GRCh38#80870253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9670353-C-A

80871629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9672396-T-C

80871689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9672456-G-C

80871844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9672586-T-C

80871934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9672686-A-G

80872027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9672778-G-A

80872175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9672913-A-G

80872359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9673097-C-T

80872844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9673747-G-A

80872910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9673813-G-A

80873313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9674154-G-A

http://identifiers.org/hco/8/GRCh38#80873402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9674217-C-A

80873402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9674217-C-T

80873484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9674274-G-A

80873484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9674274-G-C

80873484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9674274-G-T

http://identifiers.org/hco/8/GRCh38#80873488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9674278-C-A

80873516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9674303-C-T

80873594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9674380-G-A

80874292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9674986-T-G

80874355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9675052-C-G

80874403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9675100-C-G

80874523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron variant
orthologous variants: 9675208-G-A

80874523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron variant
orthologous variants: 9675208-G-T

80874644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9675327-T-C

80874666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9675349-A-G

80874678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9675361-T-C

80874861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron variant
orthologous variants: 9675509-A-G

http://identifiers.org/hco/8/GRCh38#80874886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9675530-C-A

80875634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron variant
orthologous variants: 9675853-C-T

80875642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron variant
orthologous variants: 9675862-T-G

80876163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32291
most severe consequence: intron variant
orthologous variants: 9676340-T-C