34621306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103133319-G-T

http://identifiers.org/hco/11/GRCh38#34621423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103133210-C-A

34621423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103133210-C-T

34621748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103132868-G-C

http://identifiers.org/hco/11/GRCh38#34622156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103132580-A-C

34622156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103132580-A-G

34622156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103132580-A-T

34622196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103132540-A-G

34622200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103132536-G-A

34622226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103132501-A-T

34622228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103132499-T-C

34622228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103132499-T-G

http://identifiers.org/hco/11/GRCh38#34622268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103132471-A-C

34622268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103132471-A-G

34622268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103132471-A-T

34622286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103132455-T-C

34622443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103132313-T-C

34622443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103132313-T-G

34622463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103132294-G-A

34622465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103132292-T-C

34622465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103132292-T-G

http://identifiers.org/hco/11/GRCh38#34622467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103132290-C-A

34622467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103132290-C-G

34622467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103132290-C-T

34622538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103132220-G-A

34622538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103132220-G-T

http://identifiers.org/hco/11/GRCh38#34623002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103131892-A-C

34623968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103131288-C-T

34624037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103131219-G-A

34624074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103131199-G-C

34624081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103131192-G-A

http://identifiers.org/hco/11/GRCh38#34624140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103131144-C-A

34624140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103131144-C-T

34624147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103131137-C-T

http://identifiers.org/hco/11/GRCh38#34624160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103131124-C-A

34624160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103131124-C-T

34624180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103131100-G-A

34624180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103131100-G-C

34624180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103131100-G-T

34624182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103131098-G-A

34624182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103131098-G-T

http://identifiers.org/hco/11/GRCh38#34624210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103131070-C-A

34624210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103131070-C-T

34624246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103131047-G-A

34624246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103131047-G-T

34624258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103131033-C-T

34624278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103131013-T-C

34624318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103130979-G-A

34624318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103130979-G-C

34624318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103130979-G-T

34624714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103130591-T-A

34624818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103130492-A-G

34625192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103130151-A-T

34625483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103129909-T-G

34625569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103129818-A-G

34625773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103129615-C-G

34625773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103129615-C-T

http://identifiers.org/hco/11/GRCh38#34625777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103129611-C-A

34625810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103129577-C-T

34625979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103129458-A-G

http://identifiers.org/hco/11/GRCh38#34626265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103129182-C-A

34626326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103129129-G-A

34626369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103129094-T-A

34626369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103129094-T-C

http://identifiers.org/hco/11/GRCh38#34626655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103128650-C-A

34627094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103128241-A-G

34627449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103127941-G-A

34628423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103127359-T-A

34628866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103126920-G-A

34628867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103126919-G-A

34629187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103126357-G-A

http://identifiers.org/hco/11/GRCh38#34629251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103126295-C-A

34629252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103126294-C-G

34629682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103126166-C-G

34629682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103126166-C-T

34629899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103125990-G-A

34630224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103125570-A-G

34630277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103125520-A-G

34630658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103125156-C-G

34630709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103125102-A-T

34630967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103124843-T-G

34631410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103124744-T-C

34631415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103124739-G-A

34631455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103124700-T-G

34631475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103124681-G-A

34631620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103124534-G-A

34631735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103124448-A-T

34632331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103123840-G-C

34632331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103123840-G-T

34632374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103123797-T-C

34632374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103123797-T-G

34632375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103123796-A-G

34632384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103123787-T-A

34632384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103123787-T-G

http://identifiers.org/hco/11/GRCh38#34632437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103123734-C-A

34632437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103123734-C-G

34632442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103123729-A-G

34632557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103123614-G-A

34632557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103123614-G-C

34632557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103123614-G-T

34632558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103123613-T-C

34632804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103123372-G-T

34632966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103123220-A-G

34632998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103123189-G-A

34633108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103123070-G-C

34633110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103123068-G-T

34633169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103123009-C-T

34633512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103122685-T-C

34633679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103122010-T-A

34633736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103121954-C-T

http://identifiers.org/hco/11/GRCh38#34633737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103121953-C-A

34633987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103121712-C-T

34634052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103121647-A-G

34634057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103121642-G-T

34634109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103121590-G-A

34634283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103121412-T-G

34634299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103121395-G-C

34634640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103121048-G-T

34634854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103120824-T-C

34635065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103120654-T-A

34635546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103120312-G-T

http://identifiers.org/hco/11/GRCh38#34635628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103120264-A-C

34635786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103120130-A-G

34637196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103119087-A-G

34638830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103117954-T-C

http://identifiers.org/hco/11/GRCh38#34638833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103117951-C-A

34638873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103117913-A-G

34638927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103117859-C-T

34638930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103117856-T-C

http://identifiers.org/hco/11/GRCh38#34639061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103117720-A-C

34639196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103117611-G-C

34639196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103117611-G-T

http://identifiers.org/hco/11/GRCh38#34639462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103117351-A-C

34639462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103117351-A-T

34640734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103115842-G-C

34640759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103115817-A-G

34641238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103115356-A-T

34641282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103115316-A-G

34641415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103115212-T-C

34641806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103114748-A-G

34641835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103114723-A-G

34641895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103114679-G-T

34641940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103114634-G-A

34641977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103114599-A-T

34641999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103114574-C-T

34642053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103114520-T-A

34642081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103114491-A-G

http://identifiers.org/hco/11/GRCh38#34642132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103114441-C-A

34642132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103114441-C-T

http://identifiers.org/hco/11/GRCh38#34642147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103114421-C-A

34642152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103114416-T-C

34642174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103114389-G-T

34642235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103114340-T-C

34642235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103114340-T-G

http://identifiers.org/hco/11/GRCh38#34642346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103114257-C-A

34642346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103114257-C-G

http://identifiers.org/hco/11/GRCh38#34642524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103114092-C-A

34642546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103114043-T-C

http://identifiers.org/hco/11/GRCh38#34642563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103114026-C-A

http://identifiers.org/hco/11/GRCh38#34642587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103114002-C-A

34642587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103114002-C-G

34642701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103113890-G-T

34642763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103113791-G-A

http://identifiers.org/hco/11/GRCh38#34642798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103113706-C-A

34642798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103113706-C-G

34642798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103113706-C-T

34642800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103113704-T-A

34642800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103113704-T-C

34642800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103113704-T-G

34642811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103113691-A-G

34643088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103113397-G-T

34643208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103113273-A-G

34643242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103113237-C-T

http://identifiers.org/hco/11/GRCh38#34643664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103112890-A-C

34643857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103112712-G-A

34644339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103112269-T-C

http://identifiers.org/hco/11/GRCh38#34644347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103112261-C-A

34645288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103111903-A-G

34645357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103111873-G-A

34645403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103111820-T-C

34645403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103111820-T-G

34645875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103111364-T-C

34645899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103111340-G-A

http://identifiers.org/hco/11/GRCh38#34645980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103111287-C-A

http://identifiers.org/hco/11/GRCh38#34646306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103110240-C-A

http://identifiers.org/hco/11/GRCh38#34646308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103110238-C-A

34646309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103110237-C-G

34646309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103110237-C-T

34646367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103110175-T-C

34646367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103110175-T-G

34646395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103110150-G-A

34646543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103110002-C-G

34646543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 103110002-C-T

34646681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103109864-A-G

http://identifiers.org/hco/11/GRCh38#34646689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103109856-C-A

34646741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103109837-G-C

34646755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103109823-G-A

34647268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103108678-C-T

34647480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103108499-G-C

34647482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103108497-C-T

34647690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103108354-T-C

34648537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103107628-G-A

34648551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103107614-G-T

34648636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103107521-T-C

34648811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103107368-T-C

34648813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103107366-C-T

34648860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103107316-G-A

34648860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103107316-G-T

http://identifiers.org/hco/11/GRCh38#34648887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103107292-C-A

http://identifiers.org/hco/11/GRCh38#34648962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103107222-C-A

34648962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103107222-C-T

34649139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103107057-G-T

34649351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103106860-G-A

34649808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103106158-C-T

34649863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103106102-A-G

34650156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103105848-C-T

34650157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103105847-G-A

34650310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103105700-G-A

34650855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103105177-A-G

34650855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103105177-A-T

34651026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103105015-T-C

34651229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103104776-C-T

34651385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103104623-T-C

34651514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103104493-G-A

34651514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103104493-G-T

34651675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103104349-G-A

34651725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103104309-T-C

34652039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103103995-T-C

34652088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103103947-T-C

34652511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103103549-A-G

34652666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103103406-T-G

34652999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103103097-A-G

34653025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103103073-G-A

http://identifiers.org/hco/11/GRCh38#34653419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103102742-C-A

34653419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103102742-C-T

34653530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103102634-T-A

34653645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103102459-T-C

34653719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103102390-G-A

34653731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103102378-T-C

34654211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103101898-C-G

34654211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103101898-C-T

34654943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103101190-C-T

34655079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103101050-G-A

34655427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103100720-G-T

34656081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103100058-T-A

34656081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103100058-T-C

34656105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103100027-C-G

34656105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103100027-C-T

34656188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103099308-T-C

34656438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103099067-A-G

http://identifiers.org/hco/11/GRCh38#34656455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103099049-C-A

34656521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103098970-C-T

34656527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103098963-C-G

34656641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103098823-C-G

34656641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103098823-C-T

http://identifiers.org/hco/11/GRCh38#34656758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103098692-C-A

http://identifiers.org/hco/11/GRCh38#34656818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103098639-A-C

34656818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103098639-A-T

34656834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103098623-A-G

34657235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103098335-C-T

34657887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103098025-C-T

34658069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103097876-T-C

34658198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103097765-G-T

34658243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103097722-C-T

34658386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103097613-C-G

http://identifiers.org/hco/11/GRCh38#34658395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103097604-C-A

34658673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103097365-G-A

http://identifiers.org/hco/11/GRCh38#34658767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103097265-C-A

34658767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103097265-C-G

34658767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103097265-C-T

http://identifiers.org/hco/11/GRCh38#34658787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103097257-A-C

34658787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103097257-A-G

http://identifiers.org/hco/11/GRCh38#34658992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103097053-C-A

34658992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103097053-C-G

34658992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103097053-C-T

34659207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103096834-G-T

34659301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103096740-T-C

34659301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103096740-T-G

http://identifiers.org/hco/11/GRCh38#34659339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103096698-C-A

34659478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103096563-G-T

34659489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103096552-A-G

34659560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103096491-G-T

34659751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103096335-G-T

34659814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103096272-T-C

34659815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103096271-T-A

34659882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103096204-A-G

34659882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103096204-A-T

34660030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103096074-G-T

34661290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103095717-C-T

34661607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103095411-G-A

34661607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103095411-G-T

34661655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103095363-G-A

34661759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103095248-C-T

34661817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103095189-C-T

34662005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103095025-G-T

34662464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103094601-T-C

34662875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103094186-T-C

34663075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103093992-T-A

34663075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103093992-T-C