http://identifiers.org/hco/4/GRCh38#76313362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92756460-A-C

76323400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92757916-G-A

76323821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92758221-G-A

76323935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92758310-G-T

http://identifiers.org/hco/4/GRCh38#76324058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92758419-C-A

76324089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92758450-T-A

76324174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92758531-G-C

http://identifiers.org/hco/4/GRCh38#76325090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92758900-A-C

76325273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92759091-A-T

76325279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92759097-T-G

76325280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92759098-G-A

76325496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92759292-A-G

http://identifiers.org/hco/4/GRCh38#76325693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92759510-C-A

76325747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92759559-G-T

http://identifiers.org/hco/4/GRCh38#76325834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92760281-C-A

76325834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92760281-C-T

76325846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92760293-A-G

http://identifiers.org/hco/4/GRCh38#76325905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92760352-A-C

76325907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92760354-G-A

76326008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92760455-T-C

76326026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92760473-G-A

http://identifiers.org/hco/4/GRCh38#76326066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92760511-C-A

76326066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92760511-C-T

76326184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92760600-C-T

76328205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92770767-G-C

76328363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92770910-G-T

76328370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92770922-A-G

76328770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92771122-G-A

76328770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92771122-G-C

76328770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92771122-G-T

76328865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92771207-T-C

76328865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92771207-T-G

76328913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92771241-T-C

76328928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92771256-G-A

76328928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92771256-G-C

76328943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92771271-T-C

76328961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92771289-T-A

76329038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92771766-C-T

76329240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92772120-C-T

76330174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92773387-T-A

http://identifiers.org/hco/4/GRCh38#76330267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92773470-C-A

http://identifiers.org/hco/4/GRCh38#76330352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92773564-A-C

76331163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92775105-G-A

76331163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92775105-G-T

76331181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92775123-C-G

76331181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92775123-C-T

76331236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92775175-A-G

76331237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92775176-G-A

76331237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92775176-G-T

76331290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92775229-A-T

http://identifiers.org/hco/4/GRCh38#76331313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92775246-C-A

76331326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92775259-G-A

76331326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92775259-G-T

http://identifiers.org/hco/4/GRCh38#76331469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92775586-A-C

76331469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92775586-A-G

76331502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92775619-G-A

76331502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92775619-G-T

76331519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92775690-T-C

76331919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92776648-A-G

76332037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92776752-T-C

76332321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92777386-T-C

76332399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92777424-T-A

76332405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92777430-T-G

76332512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92777531-T-C

76332697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92778244-C-G

76332987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92778496-T-C

76333014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92778523-T-A

http://identifiers.org/hco/4/GRCh38#76333111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92778918-A-C

76333215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92779011-G-A

76333496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92779272-C-T

76333571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92779530-A-T

76333823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92780105-T-C

http://identifiers.org/hco/4/GRCh38#76333870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92780152-C-A

76334036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92780288-T-C

76334036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92780288-T-G

76334068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92780323-A-G

76334093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92780348-G-A

76334182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92780436-T-C

76334183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92780437-T-C

76350979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92781138-T-C

76351049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92781208-G-A

76351049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92781208-G-C

76351052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92781211-T-C

http://identifiers.org/hco/4/GRCh38#76351107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92781266-A-C

76351107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92781266-A-G

76351174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92781331-G-T

http://identifiers.org/hco/4/GRCh38#76351690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92782062-C-A

76351690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92782062-C-T

http://identifiers.org/hco/4/GRCh38#76352014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92782368-C-A

76352080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782422-G-A

76352080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782422-G-C

76352171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782478-G-A

76352171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782478-G-T

76352187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782494-G-A

76352187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782494-G-T

http://identifiers.org/hco/4/GRCh38#76352365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92782539-C-A

76352365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782539-C-T

76352391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782553-G-T

76352401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782563-G-A

76352401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782563-G-C

76352555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782658-T-C

76352567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782671-T-C

76352569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782673-G-T

76352581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782683-G-A

76352581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782683-G-T

76352622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782725-C-T

76352670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782764-C-T

http://identifiers.org/hco/4/GRCh38#76352758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92782840-C-A

76352764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782846-G-T

http://identifiers.org/hco/4/GRCh38#76352786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92782868-C-A

76352786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782868-C-T

http://identifiers.org/hco/4/GRCh38#76352810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92782891-C-A

76352810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782891-C-T

76352846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782923-G-T

http://identifiers.org/hco/4/GRCh38#76352857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92782934-C-A

76352857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 92782934-C-T

76352880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782949-G-A

76352880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92782949-G-T

76352982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92783928-T-C

76353041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92783971-A-G

76353090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92784016-G-A

76353090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92784016-G-T

http://identifiers.org/hco/4/GRCh38#76353332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92784256-C-A

76353332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92784256-C-T

76353369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92784291-G-A

76353369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92784291-G-T

76353509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92784339-A-G

76353737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92787183-A-G

76354029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92787483-G-C

76354078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92787532-T-C

76354112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92787566-T-C

76354288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92787715-G-A

http://identifiers.org/hco/4/GRCh38#76354346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92787762-C-A

76355190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92788340-T-C

76355402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92788948-G-A

76355402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92788948-G-T

76355451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92788993-G-A

76355451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92788993-G-C

76355451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92788993-G-T

http://identifiers.org/hco/4/GRCh38#76355540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92789056-C-A

http://identifiers.org/hco/4/GRCh38#76355546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92789062-A-C

76355558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92789074-T-C

76355877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92789504-C-G

76355877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92789504-C-T

76355948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92789582-C-T

76355980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92789613-T-C

76356019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92789652-C-T

http://identifiers.org/hco/4/GRCh38#76356088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92790109-A-C

76357216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92791443-C-T

http://identifiers.org/hco/4/GRCh38#76357240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92791467-C-A

76357240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92791467-C-T

http://identifiers.org/hco/4/GRCh38#76357259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92791484-A-C

76357259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92791484-A-T

76357261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92791486-A-G

76357282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92791507-G-A

76357282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92791507-G-T

76357286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92791511-T-C

76357286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92791511-T-G

76357287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92791512-A-G

76357287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92791512-A-T

76357405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92791620-T-C

76361868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92793186-C-T

76362104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92793353-G-A

76362104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92793353-G-T

76362205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92793449-T-C

76362270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92793514-T-C

76366994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92796223-T-C

76367164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92796381-T-A

76367164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92796381-T-C

http://identifiers.org/hco/4/GRCh38#76367166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92796383-C-A

http://identifiers.org/hco/4/GRCh38#76367190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92796406-C-A

76367190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92796406-C-T

http://identifiers.org/hco/4/GRCh38#76367206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92796415-A-C

76367206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92796415-A-G

76367230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92796438-G-T

http://identifiers.org/hco/4/GRCh38#76367242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92796452-C-A

76367242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92796452-C-G

76367242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92796452-C-T

76367255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92796467-G-T

76367274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92796488-C-T

http://identifiers.org/hco/4/GRCh38#76367282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92796496-A-C

76367282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92796496-A-G

76367282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92796496-A-T

http://identifiers.org/hco/4/GRCh38#76367321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92796535-A-C

76367564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92796778-T-C

76367564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92796778-T-G

76367594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92796808-T-C

76367627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92796841-C-T

http://identifiers.org/hco/4/GRCh38#76367693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92796907-C-A

76367693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92796907-C-T

76369394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92797765-T-C

http://identifiers.org/hco/4/GRCh38#76369419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92797788-C-A

76369450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92797819-C-T

76369525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92797894-G-A

76369635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798004-G-A

76369635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798004-G-C

76369645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798013-T-A

76369645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798013-T-C

76369703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798083-G-A

76369703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798083-G-T

76369723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798100-G-A

76369723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798100-G-C

76369723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798100-G-T

http://identifiers.org/hco/4/GRCh38#76369761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92798130-C-A

76369761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798130-C-T

76371069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798225-C-T

76371262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798405-A-T

76371271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798414-T-C

76371324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798466-T-A

76371324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798466-T-G

76372461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92798922-A-G

76372547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92799003-C-T

76372548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92799004-G-A

76373207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92799610-G-A

76373680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92800076-T-C

76373701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92800094-A-G

76374177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92800574-T-C

76374468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92800789-G-C

76374502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92800809-T-C

76374515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92800822-T-C

76374592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92800940-A-G

76374876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92801197-A-G

76374895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92801243-A-G

76374941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92801289-C-T

76375185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92801558-T-A

76375185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92801558-T-G

76375190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92801563-C-T

76375289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92801652-T-C

76375289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92801652-T-G

76375352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92801721-T-C

http://identifiers.org/hco/4/GRCh38#76375504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92801832-C-A

76375504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92801832-C-T

76375586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 92801898-A-T

76375711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 92802037-T-C

76376466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92802553-G-A

76376474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92802562-A-G

http://identifiers.org/hco/4/GRCh38#76376533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92802618-A-C

76376868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92802920-G-A

76376887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92802965-G-A

76377486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92803723-G-A

76377551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92803787-C-T

76377571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92803805-A-T

76377716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92803904-T-C

76377980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92804139-G-A

76377980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92804139-G-T

76378325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92804467-T-C

http://identifiers.org/hco/4/GRCh38#76378821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92805208-A-C

http://identifiers.org/hco/4/GRCh38#76379269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92805702-A-C

76379419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92805855-G-C

76379419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92805855-G-T

76379493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92805933-C-G

76379493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92805933-C-T

76379496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92805936-G-T

76379498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92805938-T-C

76379498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92805938-T-G

76379515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92805955-T-A

76379523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92805963-A-G

http://identifiers.org/hco/4/GRCh38#76382567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92807490-C-A

76382567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92807490-C-T

76382672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92807604-A-G

76382683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92807615-T-A

76382750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92807681-G-A

76382750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92807681-G-T

76382811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92807738-A-G

76382987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92808795-A-G

76382994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92808802-T-C

76383209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92808969-C-G

http://identifiers.org/hco/4/GRCh38#76383317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92809073-A-C

76383652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92809382-A-G

76383903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92809627-C-T

76383947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92809672-G-T

76383948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92809673-A-G

76383968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92809682-T-C

76384246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92809942-G-A

76384246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92809942-G-T

76384247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92809943-G-T

76384325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92810021-G-T

76384360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92810056-G-T

76384375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92810071-G-A

76384438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92810134-T-C

http://identifiers.org/hco/4/GRCh38#76384487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92810324-C-A

76384487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92810324-C-G

76384487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92810324-C-T

76384561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92810497-G-A

76384689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92810632-T-G

http://identifiers.org/hco/4/GRCh38#76384696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92810642-C-A

76384817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92810696-T-C

76384817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92810696-T-G

76384901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92810733-G-A

76384961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92810823-A-G

http://identifiers.org/hco/4/GRCh38#76385010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92810864-C-A

76385068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92811160-C-T

76395143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92813563-C-T

76395313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92813742-G-C

76395470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92813864-A-G

76395514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92813908-T-C

76395940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92814272-C-G

76395940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92814272-C-T

76396028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92814355-A-G

http://identifiers.org/hco/4/GRCh38#76396063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92814383-A-C

http://identifiers.org/hco/4/GRCh38#76396125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92814429-C-A

76396125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92814429-C-G

http://identifiers.org/hco/4/GRCh38#76396147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92814449-C-A

76396162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92814463-G-T

76402900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92816287-A-G

http://identifiers.org/hco/4/GRCh38#76403026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92816408-C-A

76403026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92816408-C-T

http://identifiers.org/hco/4/GRCh38#76403038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92816420-C-A

76403119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92816512-T-G

76403131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 92816524-C-T

76403151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: non_coding_transcript_exon_variant, stop_gained, synonymous_variant
orthologous variants: 92816544-G-T

http://identifiers.org/hco/4/GRCh38#76403255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92816642-C-A

76403301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92816689-A-G

http://identifiers.org/hco/4/GRCh38#76403326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92816709-A-C

76403843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92817416-T-G

76403887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92817465-C-T

76403911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92817489-A-G

76403960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92817549-G-A

76403960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92817549-G-T

76404034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92817599-G-A

76404034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92817599-G-T

76404135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92817677-G-A

76409171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92818716-C-G

76409171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92818716-C-T

76410009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92819283-C-T

76411105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92819931-A-G

76411702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92820220-T-C

76412259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92820680-A-G

76420122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92822211-C-T

http://identifiers.org/hco/4/GRCh38#76420408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92822456-A-C

76420646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92822647-G-A

76420646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92822647-G-T

76420651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92822652-A-G

76420736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92822714-G-A

76420833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92822800-G-A

76420866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92822828-C-T

76420890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92822851-A-T

http://identifiers.org/hco/4/GRCh38#76420919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92822881-C-A

76421008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92822960-G-A

76421008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92822960-G-T

76421028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92822969-G-A

76421047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92822988-T-A

76421047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92822988-T-G

76421052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92822993-G-T

76421129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92823040-G-A

76421141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92823050-T-G

76421170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92823085-G-C

76421230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92823116-G-C

76421415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92823302-C-T

76421424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92823311-A-G

76421457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92823371-G-A

76421463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92823376-T-C

76421603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 92823540-T-C

http://identifiers.org/hco/4/GRCh38#76421605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92823545-C-A

76421605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92823545-C-T

http://identifiers.org/hco/4/GRCh38#76421656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92823579-A-C

76421656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92823579-A-G

76421656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92823579-A-T

http://identifiers.org/hco/4/GRCh38#76421677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92823600-A-C

76421677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92823600-A-G

76421677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92823600-A-T

http://identifiers.org/hco/4/GRCh38#76421690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92823613-A-C

76421690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92823613-A-G

76421690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92823613-A-T

76421733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 92823632-G-A

http://identifiers.org/hco/4/GRCh38#76421759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92823687-C-A

76421770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 92823701-A-G

76421770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 92823701-A-T

http://identifiers.org/hco/4/GRCh38#76421794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92823722-C-A

76421795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 92823723-G-A

76421795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26374
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 92823723-G-T