66480165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4978582-G-A

66480179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4978568-G-A

66480179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4978568-G-T

66480215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4978513-G-A

66480215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4978513-G-C

66480215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4978513-G-T

66480256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4978459-G-A

66480256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4978459-G-C

66480256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4978459-G-T

http://identifiers.org/hco/11/GRCh38#66480257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4978458-C-A

66480475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4978236-G-A

66480555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4978154-T-C

66480558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4978151-G-A

66480558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4978151-G-T

http://identifiers.org/hco/11/GRCh38#66480565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4978144-C-A

http://identifiers.org/hco/11/GRCh38#66480590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4978119-C-A

66480590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4978119-C-T

66480687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4978032-G-A

66480687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4978032-G-T

66480689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4978030-G-A

66480689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4978030-G-T

66480934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4977811-G-A

66480934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4977811-G-T

66480941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4977804-G-T

66480942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4977803-A-G

http://identifiers.org/hco/11/GRCh38#66480955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4977790-C-A

66480955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4977790-C-G

66480955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4977790-C-T

66481089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4977553-T-C

66481090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4977552-G-A

66481125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4977526-G-A

66481212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4977430-G-C

http://identifiers.org/hco/11/GRCh38#66482039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4977231-C-A

66482039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4977231-C-G

http://identifiers.org/hco/11/GRCh38#66482054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4977220-C-A

66482094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4977181-G-A

66482094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4977181-G-T

66482151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4977121-T-C

http://identifiers.org/hco/11/GRCh38#66482190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4977091-C-A

66482190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 4977091-C-T

66482273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4977008-C-T

66482330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4976951-G-A

66482330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 4976951-G-T

66482513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4976770-G-T

66482656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4976613-C-G

66482911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4976335-C-G

66482911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4976335-C-T

66482919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4976327-C-G

66482933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4976313-A-G

66482964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4976286-A-G

http://identifiers.org/hco/11/GRCh38#66483150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4976117-C-A

66484656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4974060-G-C

66484982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4973991-G-A

http://identifiers.org/hco/11/GRCh38#66485343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4973655-A-C

66485343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4973655-A-G

66485343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4973655-A-T

http://identifiers.org/hco/11/GRCh38#66486423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4973321-C-A

66486423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4973321-C-G

66486423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4973321-C-T

66486504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4973267-G-A

66486504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4973267-G-T

http://identifiers.org/hco/11/GRCh38#66486511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4973260-C-A

66486511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4973260-C-T

66486540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 4973230-G-A

66486540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, stop_gained
orthologous variants: 4973230-G-T

http://identifiers.org/hco/11/GRCh38#66486552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4973218-C-A

66486552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4973218-C-T

66486584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4973186-G-A

66486584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4973186-G-T

66486597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4973173-G-A

http://identifiers.org/hco/11/GRCh38#66486639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4973131-C-A

66486728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4973047-A-G

66486730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4973045-G-A

66486730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4973045-G-T

66486765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4973008-A-G

66486795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4972980-G-T

66486870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4972936-G-A

66486991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4972830-G-C

66486991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4972830-G-T

66487198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4972512-G-C

66487213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4972490-T-G

66487246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4972456-T-C

66487261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 4972429-C-T

66487799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4971366-G-A

66487799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4971366-G-T

66487955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: missense variant
orthologous variants: 4971219-T-A

66487955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: synonymous variant
orthologous variants: 4971219-T-C

66488028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4971146-C-T

66488062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4971121-G-A

66488062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4971121-G-T

66488063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4971120-G-A

66488090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4971095-C-T

66488151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4971037-T-A

66488151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4971037-T-C

66488217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4970981-C-G

66491048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4968623-C-T

http://identifiers.org/hco/11/GRCh38#66491115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4968487-C-A

66491115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4968487-C-T

66491176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4968434-T-C

66491176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4968434-T-G

66491182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4968428-A-G

66491261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: missense variant
orthologous variants: 4968393-C-G

66491261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: synonymous variant
orthologous variants: 4968393-C-T

66491480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, undefined
orthologous variants: 4968191-C-T

66491566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: missense variant
orthologous variants: 4968104-G-A

66491569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: missense variant
orthologous variants: 4968101-G-A

66491581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: missense variant
orthologous variants: 4968089-G-A

66491644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4968016-C-T

66491645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4968015-C-G

66491645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4968015-C-T

http://identifiers.org/hco/11/GRCh38#66491646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4968014-A-C

66491997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4967717-G-A

66492067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4967659-G-A

http://identifiers.org/hco/11/GRCh38#66492250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4967504-C-A

66492264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4967490-T-C

http://identifiers.org/hco/11/GRCh38#66492283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4967472-C-A

66492283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4967472-C-T

http://identifiers.org/hco/11/GRCh38#66492318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4967460-A-C

66492337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4967443-A-G

66492337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4967443-A-T

66492344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4967436-A-G

66492355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4967425-T-C

http://identifiers.org/hco/11/GRCh38#66492363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4967417-C-A

http://identifiers.org/hco/11/GRCh38#66492378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4967404-C-A

66492378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4967404-C-G

66492378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4967404-C-T

66492381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4967401-T-A

66492381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4967401-T-C

66492381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4967401-T-G

66492427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4967360-T-C

66492427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4967360-T-G

66492438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4967349-G-A

66492438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4967349-G-T

66492475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4967331-G-A

66492475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4967331-G-C

66492492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4967311-A-G

http://identifiers.org/hco/11/GRCh38#66492532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4967284-C-A

66492532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4967284-C-G

66492543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4967273-C-T

http://identifiers.org/hco/11/GRCh38#66492564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4967263-A-C

66492564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4967263-A-G

66492571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4967256-A-G

66492644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4967185-A-G

66492662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4967159-A-G

66492663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4967158-G-A

66492682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4967143-C-T

66492683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4967142-C-T

66492703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4967122-C-T

http://identifiers.org/hco/11/GRCh38#66492807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4967021-C-A

66492807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4967021-C-G

66492807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4967021-C-T

66492829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4966999-T-C

66493069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 4966834-G-A

66493069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 4966834-G-C

66493136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4966767-C-T

66493168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4966735-G-A

66493190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4966713-G-A

66493190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4966713-G-T

66493214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4966691-C-G

66493236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4966680-G-A

66493282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4966640-A-G

66493312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4966612-G-A

66493312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4966612-G-T

66493409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4966521-G-T

http://identifiers.org/hco/11/GRCh38#66493483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4966457-C-A

66493483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4966457-C-T

66493507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4966430-A-G

66493705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4966269-G-A

66493705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4966269-G-T

66494178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4965940-A-G

66494541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4965585-G-A

66494541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4965585-G-C

66494555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4965571-G-A

66494840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4965320-G-A

66495173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4965124-G-A

66495173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4965124-G-T

66495263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4965050-G-A

66495287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4965027-G-A

http://identifiers.org/hco/11/GRCh38#66495414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4964911-C-A

66495428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4964897-T-C

66495520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4964801-T-C

66495521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4964800-C-G

66495521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4964800-C-T

66495526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4964795-T-C

66495567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4964774-G-T

66495755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4964601-G-A

66495756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4964600-G-T

66495778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4964596-G-T

66497153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4964088-T-G

66497184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4964063-A-G

66497188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4964059-G-A

66497188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4964059-G-T

66497231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4964045-A-G

66497232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4964044-A-G

66497263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4964008-G-A

66497263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4964008-G-T

http://identifiers.org/hco/11/GRCh38#66497269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4964002-C-A

66497269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4964002-C-T

66497394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: missense variant
orthologous variants: 4963882-C-T

66497557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4963674-G-T

66504522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron variant
orthologous variants: 4960124-G-A

66504636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: missense variant
orthologous variants: 4960010-G-A

66504639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: missense variant
orthologous variants: 4960007-G-A

http://identifiers.org/hco/11/GRCh38#66504777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4959869-A-C

http://identifiers.org/hco/11/GRCh38#66504878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4959807-C-A

66504878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959807-C-G

66504878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959807-C-T

66504904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959786-T-A

66504904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959786-T-C

66507563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959253-G-A

66508213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4958679-A-G

66508214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4958678-G-A

http://identifiers.org/hco/11/GRCh38#66508316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4958614-C-A

66508316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4958614-C-T

http://identifiers.org/hco/11/GRCh38#66508341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4958596-A-C

66508457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4958460-A-G

66508964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4957894-G-A

66508964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4957894-G-T

http://identifiers.org/hco/11/GRCh38#66508972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#4957886-C-A

66509045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4957856-T-G

http://identifiers.org/hco/11/GRCh38#66509217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#4957685-A-C

66509231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4957668-G-A

66509231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4957668-G-T

66509339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3008
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 4957565-G-C