110643298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53664853-T-C

110643673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53665131-G-A

110643998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53665389-G-A

110644220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53665590-G-A

110644302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53665686-A-G

110644316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53665700-G-A

110644316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53665700-G-C

110644316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53665700-G-T

110644433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53665817-T-C

110644530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, missense_variant
orthologous variants: 53665914-G-A

110644530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, missense_variant
orthologous variants: 53665914-G-T

110644553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 53665937-G-A

110644553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 53665937-G-C

110644553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 53665937-G-T

110644583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 53665967-G-A

110644583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, missense_variant
orthologous variants: 53665967-G-T

110644660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53666037-G-T

http://identifiers.org/hco/10/GRCh38#110644745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53666120-C-A

110644745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53666120-C-T

110644766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53666141-T-C

110644843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53666237-T-C

110645187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53666579-T-C

110645254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53666612-C-T

110645283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53666640-G-A

110645580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53666895-T-C

110645801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53667127-A-G

110645967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53667279-G-A

110646003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53667310-T-C

110646239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53667539-A-G

110646431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53667730-G-C

110646432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53667731-C-G

110647266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53668525-G-C

110647527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53668816-T-C

http://identifiers.org/hco/10/GRCh38#110647900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53669166-A-C

110647925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53669191-A-T

110648040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53669303-G-A

110648161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53669400-G-A

110648161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53669400-G-T

110648278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53669504-G-A

110648482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53669680-C-G

110648482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53669680-C-T

110648815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53670009-T-C

110649215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53670391-T-C

110649215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53670391-T-G

110649272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53670427-G-C

110649308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53670463-T-C

110649390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53670554-A-G

110649483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53670649-G-T

110649745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53670805-A-G

110649936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53670987-A-T

110650165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53671169-C-T

http://identifiers.org/hco/10/GRCh38#110650413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53671378-C-A

http://identifiers.org/hco/10/GRCh38#110650609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53671576-C-A

110651005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53672202-C-T

110651066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53672270-A-G

110651541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53672661-A-G

110651735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53672825-C-T

110651775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53672868-G-T

110651794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, undefined
orthologous variants: 53672887-T-G

http://identifiers.org/hco/10/GRCh38#110658149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53675956-C-A

110658149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53675956-C-G

110658234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53676037-C-G

110658234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53676037-C-T

110658259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53676062-C-G

110658259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53676062-C-T

110658279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53676081-G-A

110658501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53676297-C-G

110658594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53676392-C-T

110658700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53676828-G-A

http://identifiers.org/hco/10/GRCh38#110658744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53676872-C-A

110658744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53676872-C-G

110658848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53677015-G-C

110659154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53678598-A-T

110659198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53678636-T-A

110659244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53678681-T-G

110659319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53678749-C-T

110661184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53680998-T-C

110661194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53681008-A-T

110661453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53681255-A-T

110661471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53681273-T-C

110661616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53681419-A-G

110661688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53681478-A-G

110662308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53681757-G-A

http://identifiers.org/hco/10/GRCh38#110662377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53681806-A-C

110662457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53681876-C-T

110662477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53681896-T-G

110666048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53684316-G-A

110666223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53684498-T-C

110667138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53685367-T-C

110667278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53685499-G-A

110667345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53685552-G-A

110667345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53685552-G-T

110667531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53685742-G-A

110667612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53685823-T-C

110667613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53685824-G-T

110667652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53685871-A-G

110667672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53685885-G-A

http://identifiers.org/hco/10/GRCh38#110667706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53685922-C-A

110667706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53685922-C-G

110667968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53686137-T-C

110668221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, undefined
orthologous variants: 53686391-C-T

110668244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53686436-T-C

http://identifiers.org/hco/10/GRCh38#110668319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53686541-A-C

110668368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53686582-C-T

110668431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, undefined
orthologous variants: 53686637-C-T

110668749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53686892-A-T

110669386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53688049-A-T

110669390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53688053-G-C

110669411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53688074-G-A

http://identifiers.org/hco/10/GRCh38#110669506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53688185-A-C

110669506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53688185-A-G

110669507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53688186-A-G

110669915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53688425-T-A

110669915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53688425-T-C

110669921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53688429-G-T

110670400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53688800-C-G

110670400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53688800-C-T

110674240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53694986-T-C

110674241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53694987-A-G

110674313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53695034-C-T

110674534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53695254-C-G

110674746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53695447-A-G

110674869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53695573-G-A

110674938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53695617-G-A

110674938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53695617-G-T

110675098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53695769-C-T

110675112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53695785-T-C

110675242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53696088-C-T

110675244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53696090-T-C

110675402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53696421-G-A

110675404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53696423-G-A

110675994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53696795-G-T

110676044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, undefined
orthologous variants: 53696852-G-A

110676447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53697194-A-G

110676497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53697241-G-A

110676525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53697272-T-C

110676572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53697319-T-A

110676572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53697319-T-C

110676799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53697993-T-G

110679520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53699207-C-T

110679576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53699263-A-T

110679858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53699519-A-G

110680002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53699653-T-C

110680112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53699741-C-T

http://identifiers.org/hco/10/GRCh38#110680173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53699800-C-A

110680194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53699820-G-A

110680194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53699820-G-C

110680304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53699924-C-T

110680396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53700012-C-T

110680397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53700013-A-G

http://identifiers.org/hco/10/GRCh38#110680482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53700094-C-A

110680686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53700280-G-A

110680757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53700356-T-C

110680779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53700376-G-C

110680786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53700383-G-A

110680883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53700486-C-G

110680887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53700490-C-T

110681199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, undefined
orthologous variants: 53700926-G-A

110681463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53701148-T-G

110681466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53701151-T-G

110681698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53701381-G-A

110681760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53701442-T-C

110682330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53701879-G-A

110682432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53701976-T-G

110682481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53702015-T-A

110682498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53702031-G-A

110682531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53702064-C-T

110682841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53702339-T-A

110683040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53702517-C-G

110683052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53702531-T-C

110683401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53703015-G-T

110683525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53703133-T-G

110683534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53703142-G-T

110683567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53703159-G-A

110683661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53703211-T-C

110683662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53703212-G-A

110683910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53703643-G-A

110683956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53703693-A-G

110683994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53703730-A-G

110684073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53703808-A-G

110684083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53703822-A-G

110684838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53704231-T-A

110684838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53704231-T-C

110684867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53704266-G-A

http://identifiers.org/hco/10/GRCh38#110685086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53704844-C-A

110685131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53704902-C-T

http://identifiers.org/hco/10/GRCh38#110685137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53704908-C-A

110685137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53704908-C-T

110685138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53704909-G-A

110685157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53704927-C-T

110685224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, undefined
orthologous variants: 53704994-C-G

110685251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53705018-A-G

110685266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53705034-G-T

110685432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, undefined
orthologous variants: 53705191-G-T

110685517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53705273-A-G

110685727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53705636-A-T

110685729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53705638-T-G

110685736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53705645-G-C

110685775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53705678-G-A

110685962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53705857-A-G

110686238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53706417-G-T

110687590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53708159-T-C

110687610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53708179-A-T

110687672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53708241-C-T

110687748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53708317-C-T

110687833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53708394-C-T

110688070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53708702-G-A

110688158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53708785-C-G

110688180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53708807-T-C

110688406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53708986-A-G

110693547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53712842-G-C

110693547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53712842-G-T

110693670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53712957-G-T

110693686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53712973-G-T

110693696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53712981-A-G

110693858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53713258-G-A

110693868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53713268-A-G

110693940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53713343-G-T

110694257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53713626-T-C

110694410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53713773-T-C

110694454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53713810-A-G

110694478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53713835-A-T

110694500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53713857-A-G

110694610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53713971-G-C

110694689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53714050-A-G

http://identifiers.org/hco/10/GRCh38#110694810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53714157-C-A

110695033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53714520-A-G

110695122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53714612-G-A

110695122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53714612-G-C

110695203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53714691-G-A

110695203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53714691-G-T

110695206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53714694-T-A

110695206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53714694-T-C

110695285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53714765-A-T

110695431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53714910-T-C

110695668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53715149-G-C

http://identifiers.org/hco/10/GRCh38#110695903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53715382-A-C

110695958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53715429-T-C

110696142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53715621-G-A

110696142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53715621-G-C

110696173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53715652-T-C

110696253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53715761-C-T

110696301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53715803-A-G

110696334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53715828-T-C

110696334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53715828-T-G

110696389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53715883-G-A

110696729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53716213-A-T

http://identifiers.org/hco/10/GRCh38#110697662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53717418-C-A

110697901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53717612-C-T

http://identifiers.org/hco/10/GRCh38#110698308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53717929-C-A

110698458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53718073-G-C

110698566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53718180-A-G

110698667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53718290-C-T

110698690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53718314-T-C

110698949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53718548-G-T

110699129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53718726-G-A

110699240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53718819-T-C

110700198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53718883-C-G

110700242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53718937-C-T

110700460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53719166-A-T

110700702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53719382-A-G

110701158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53719720-A-G

110701161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53719724-T-C

110701260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53719818-C-T

110701443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53719983-A-T

110701466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53720006-G-A

110701476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53720023-C-T

110701522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53720069-G-C

110701557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53720106-C-T

110701645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53720232-A-G

110701839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53720422-G-A

110701839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53720422-G-T

110701996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53720562-G-A

110702106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53720672-T-C

110702242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53720787-A-G

110704780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53725454-A-T

110704949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53725638-A-G

110704950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53725639-T-C

110705856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53726417-G-A

110705875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53726427-G-A

110705975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53726557-G-T

110705977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53726559-G-A

110706017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53726578-T-G

110706092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53726637-G-A

110706092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53726637-G-T

110706110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53726655-C-T

110706230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53726792-G-C

110706907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, undefined
orthologous variants: 53727442-T-G

http://identifiers.org/hco/10/GRCh38#110707026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53727548-A-C

110707026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53727548-A-G

110707029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53727551-T-G

110709301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53728618-G-A

110710923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53729088-C-G

110710997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53729533-G-A

110711053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53729595-G-A

110711053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53729595-G-C

110711606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53730059-A-G

110712380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53731118-G-A

110712854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53731418-A-G

110713141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53731672-T-C

110716164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53731932-C-T

110716255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53732018-C-T

110716596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53732381-G-A

110716810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53732707-G-C

110717549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53733299-G-A

http://identifiers.org/hco/10/GRCh38#110717609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53733353-C-A

110717719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53733459-T-C

110717778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53733498-G-C

110717885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53733583-G-C

110718051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53733720-C-G

110718051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53733720-C-T

110718317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53733923-C-T

110718364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53733962-T-A

110718546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53734062-T-A

http://identifiers.org/hco/10/GRCh38#110718605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53734124-A-C

110718605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53734124-A-T

110720883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53736279-A-G

110720942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53736327-C-G

110720996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53736380-C-T

110721071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53736442-C-G

110721194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53736553-A-G

110721255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53736617-C-G

110721365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53736725-C-G

110721420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53736780-C-T

110721537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53736842-A-G

110721543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53736848-C-T

110721820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53737117-G-A

110721922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53737205-A-G

110722054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53737467-G-A

110722124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53737529-C-G

110722249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53737632-T-C

110722700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53738374-T-C

http://identifiers.org/hco/10/GRCh38#110722716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53738389-C-A

110722720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53738393-A-G

110722781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53738447-G-A

110723869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53738917-T-C

110723946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53738991-A-G

110724103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53739837-T-C

110724103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53739837-T-G

110724664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53740352-G-A

110724862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53740544-G-C

110725004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53740688-C-G

110725188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53740855-T-C

110725189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53740856-G-A

110725529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53742340-A-G

110725794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53742826-G-T

110725812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53742844-C-T

110725860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53742941-G-A

110725860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53742941-G-T

110725925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53743005-C-T

http://identifiers.org/hco/10/GRCh38#110726272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53743313-A-C

110726552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53743562-A-G

http://identifiers.org/hco/10/GRCh38#110726757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53743744-C-A

110726757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53743744-C-G

110726761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53743748-G-A

110726797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53743785-A-G

110728283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53744002-T-C

110728694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53744343-G-A

110728727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53744360-G-A

110728849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53744479-T-A

110728862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53744492-C-T

110728869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53744493-C-T

110728970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53744605-T-A

110729334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53744941-G-A

http://identifiers.org/hco/10/GRCh38#110732637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53745230-C-A

110732637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53745230-C-T

110732705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53745279-A-G

http://identifiers.org/hco/10/GRCh38#110732711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53745285-C-A

110732755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53745325-G-T

110732953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53745589-A-G

110733119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53745828-G-A

110733172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53745881-G-T

110733338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53745980-G-A

110733388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53746024-C-T

110733415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53746050-T-C

110733422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53746057-T-A

110733570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53746178-C-G

110733641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53746233-T-G

110733657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53746249-T-C

110734025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53746554-G-T

110734092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53746605-G-A

110734221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53746736-C-G

110739287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53747608-C-T

110739329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53747668-T-G

110740036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, undefined
orthologous variants: 53748762-C-G

110740036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, undefined
orthologous variants: 53748762-C-T

110740173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53748870-T-C

http://identifiers.org/hco/10/GRCh38#110740305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#53748976-A-C

110740442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53749123-G-A

http://identifiers.org/hco/10/GRCh38#110740586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53749248-C-A

110740628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53749282-A-T

http://identifiers.org/hco/10/GRCh38#110740643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53749297-C-A

110740643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53749297-C-T

110740698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53749348-G-C

110740721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53749371-C-G

110740773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53749423-C-G

110740837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53749467-T-C

110740918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53749544-T-C

110740979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53749606-C-T

110740980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53749607-A-G

110741008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53749635-G-A

110741149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53749766-C-T

110742331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53750353-T-C

110742384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53750404-G-A

110742417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53750428-G-C

110746358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53756899-A-T

110746388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53756923-G-C

110746388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53756923-G-T

110746435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53756969-G-A

http://identifiers.org/hco/10/GRCh38#110746570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#53757100-C-A

110746570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53757100-C-G

110746570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53757100-C-T

110746571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53757101-G-A

110746572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53757102-A-T

110747011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53758326-T-C

110747157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759579-T-G

110747228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759642-G-C

http://identifiers.org/hco/10/GRCh38#110747249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53759670-C-A

110747252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759673-C-G

110747295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759742-T-G

110747298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759745-G-A

110747298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759745-G-C

110747298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759745-G-T

110747320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759762-G-C

110747340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759780-C-G

110747340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759780-C-T

110747643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53759994-G-A

110747643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53759994-G-T

110747965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53760473-G-A

110748030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53760539-A-G

110748172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53760682-A-G

110748233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53760740-A-G

110748439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53760905-T-C

110748506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53760962-C-T

110748545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53761001-G-C

110748904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53761314-C-T

110749972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53767387-G-A

110750057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53767468-A-G

http://identifiers.org/hco/10/GRCh38#110750365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53767865-C-A

110750375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53767875-G-A

110750419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53767911-G-T

110751015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53768339-C-T

110751016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53768340-G-A

110751053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53768359-C-T

110755421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53773327-T-A

110755540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53773450-G-A

110755731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53773714-C-T

http://identifiers.org/hco/10/GRCh38#110755847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53773832-C-A

110755847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53773832-C-T

110755977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53773967-G-A

110755977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53773967-G-T

110756042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53774028-A-T

110756079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53774065-A-G

http://identifiers.org/hco/10/GRCh38#110756258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53774592-C-A

110756258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53774592-C-T

110756283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53774616-G-A

110756432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53774764-A-G

110756433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53774765-G-A

110756438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53774770-A-T

110756441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53774773-G-A

http://identifiers.org/hco/10/GRCh38#110756446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53774778-C-A

110756446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53774778-C-T

110756453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53774785-G-A

http://identifiers.org/hco/10/GRCh38#110756843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53775027-C-A

110756843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53775027-C-T

http://identifiers.org/hco/10/GRCh38#110756859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53775033-C-A

110757037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53775209-A-G

110757695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53775795-G-T

110757828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53775931-G-A

110758773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53777274-A-T

110758774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53777275-A-G

110758784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53777285-T-C

110758955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53777433-G-C

110758987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53777465-A-G

http://identifiers.org/hco/10/GRCh38#110759032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53777510-C-A

110759077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53777556-C-G

110759106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53777580-T-G

http://identifiers.org/hco/10/GRCh38#110759276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53777737-C-A

110759276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53777737-C-G

110759355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53777857-G-A

110759355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53777857-G-C

110759628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53778107-C-G

110759826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53778292-C-T

110760005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53778492-G-A

110760138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53778596-T-G

110760206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53778663-C-G

110760206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53778663-C-T

110760277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53778739-C-T

110760386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53778835-G-A

110760386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53778835-G-C

http://identifiers.org/hco/10/GRCh38#110761648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53779375-C-A

110761648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53779375-C-T

http://identifiers.org/hco/10/GRCh38#110761738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53779468-A-C

110761791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53779522-T-G

110761793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53779524-G-A

110761830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53779562-G-T

110761931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53779582-G-A

110762264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53779682-T-C

110762531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53779889-C-T

110762898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53780151-G-C

110762899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53780152-A-T

110762935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53780184-A-T

110762958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53780205-G-C

110762982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53780222-G-T

110763114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53780332-C-G

110763258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53780511-G-T

110763334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53780612-G-T

110763406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53780672-T-C

110763651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53780878-G-A

110763651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53780878-G-T

110763680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53780906-C-T

http://identifiers.org/hco/10/GRCh38#110763689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53780915-C-A

110763689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53780915-C-G

110763752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53780968-T-C

110764022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53781100-T-G

http://identifiers.org/hco/10/GRCh38#110764308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53781354-A-C

110764382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53781427-G-A

http://identifiers.org/hco/10/GRCh38#110764391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53781436-C-A

110764391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53781436-C-T

110764630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53781675-T-G

110764875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53781930-C-T

110765184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53782192-T-C

http://identifiers.org/hco/10/GRCh38#110765204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53782214-C-A

110765392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53782383-A-G

110765488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53782481-T-C

110765780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53782771-C-T

110766297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53783308-A-T

110768282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53783328-T-C

110768282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53783328-T-G

110768301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53783352-T-G

110768522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53783574-T-C

110769214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53784031-A-T

110769302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53784110-G-A

110769387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53784184-C-G

110769387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53784184-C-T

110769448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53784239-T-G

110769498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53784266-C-G

110769785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53784520-C-G

110770541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53785146-C-G

110770588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53785198-A-G

110770790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53785389-G-A

110770886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53785475-C-T

110770887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53785476-G-A

110770985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53785546-G-A

110771123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53785646-G-A

110771123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53785646-G-C

110771124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53785647-C-T

110771803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53785973-A-G

110771913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53786076-C-T

110772138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53786308-C-T

110772144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53786314-C-T

110772215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53786381-A-G

110773188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53787094-C-T

110773695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53788440-G-A

110774216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53789033-G-C

110774267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53789085-A-T

110774542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53789341-C-G

110774643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53789436-G-A

110774800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53789549-C-T

110774855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53789605-C-T

110774891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53789641-G-A

110775241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53790104-C-G

110775241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53790104-C-T

110775579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53790431-T-C

110775628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53790478-C-T

110775635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53790485-C-T

110776738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53796278-G-T

110776853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53796521-G-A

110776913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53796573-G-T

110777020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53796645-G-T

110777095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53796718-C-T

110777183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53796795-T-C

110777380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53797211-G-A

110777410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53797241-G-A

110777411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53797242-G-A

http://identifiers.org/hco/10/GRCh38#110777587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53797426-C-A

110777828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53797719-C-G

http://identifiers.org/hco/10/GRCh38#110777914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53797804-A-C

110777980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53797846-A-G

110778601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53798745-C-T

http://identifiers.org/hco/10/GRCh38#110778642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53798784-A-C

110778960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53799085-C-G

110780685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53801564-G-C

110780685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53801564-G-T

http://identifiers.org/hco/10/GRCh38#110780724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53801603-C-A

http://identifiers.org/hco/10/GRCh38#110780741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53801620-C-A

110780741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53801620-C-T

http://identifiers.org/hco/10/GRCh38#110780746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53801625-C-A

110780746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53801625-C-T

http://identifiers.org/hco/10/GRCh38#110780756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53801633-C-A

110780756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53801633-C-G

110780756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53801633-C-T

110780861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 53801739-T-C

110781029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53801907-G-A

110781029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53801907-G-T

http://identifiers.org/hco/10/GRCh38#110781084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53801962-A-C

110781084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53801962-A-G

110781092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53801970-T-C

110781149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53802027-C-T

110781315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53802193-T-C

110781326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53802204-A-G

110781326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53802204-A-T

110781347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53802225-T-C

110781347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53802225-T-G

110781399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53802283-G-A

110781463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53802347-C-T

110781482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53802366-T-C

110781483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53802367-G-T

110781510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53802394-G-A

110781510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53802394-G-C

http://identifiers.org/hco/10/GRCh38#110781764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53802651-C-A

http://identifiers.org/hco/10/GRCh38#110781941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53802798-C-A

110781941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53802798-C-G

110781941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53802798-C-T

110782033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53802887-A-G

110782178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53802971-G-A

http://identifiers.org/hco/10/GRCh38#110782220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53803012-C-A

110782220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53803012-C-T

110782227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53803019-T-C

110782280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53803074-A-G

110782288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53803082-A-G

110782979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53803610-T-A

110783054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53803648-T-G

110783109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53803698-T-C

110783219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53803809-A-G

110783222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53803812-G-A

110783227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53803815-G-A

110783227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53803815-G-T

110783355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53803941-T-C

110783386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53803967-A-G

http://identifiers.org/hco/10/GRCh38#110783551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53804113-C-A

110783561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53804123-A-G

110783569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53804131-G-T

110783802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53805100-C-T

110783950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53805181-C-T

110783951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53805182-G-A

110784007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53805240-G-A

110784007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53805240-G-C

110784008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53805241-T-C

110784027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53805260-T-A

110784027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53805260-T-C

110784198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53805413-A-G

http://identifiers.org/hco/10/GRCh38#110784213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53805424-C-A

110784231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53805462-C-G

110784231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53805462-C-T

110784232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53805463-T-G

http://identifiers.org/hco/10/GRCh38#110784262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53805492-C-A

110784262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53805492-C-G

110784262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53805492-C-T

110784301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53805529-A-G

110784367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53805603-C-T

110784368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53805604-G-A

110784399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53805635-A-G

http://identifiers.org/hco/10/GRCh38#110784498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53805730-C-A

110784504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53805736-T-C

110784504-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53805736-T-G

http://identifiers.org/hco/10/GRCh38#110784517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53805748-C-A

http://identifiers.org/hco/10/GRCh38#110784897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53806459-C-A

110784897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 53806459-C-T

110784898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53806460-G-A

110786210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, undefined
orthologous variants: 53807825-G-A

110786210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, undefined
orthologous variants: 53807825-G-T

110786337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, undefined
orthologous variants: 53807911-G-A

110786337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, undefined
orthologous variants: 53807911-G-C

110787002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53808219-G-A

110787031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53808235-A-G

110787276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53808481-C-T

http://identifiers.org/hco/10/GRCh38#110787279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53808484-C-A

110787301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53808511-G-A

110787367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53808567-G-A

110787395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53808605-A-G

http://identifiers.org/hco/10/GRCh38#110787561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53808705-A-C

110787617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53808749-C-T

110787628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53808761-G-A

110787628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53808761-G-T

110787677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53808824-C-T

110787944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53808967-G-A

110787954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53808977-A-T

http://identifiers.org/hco/10/GRCh38#110787966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53808989-C-A

110788213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53809230-C-T

110788261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53809306-G-A

http://identifiers.org/hco/10/GRCh38#110788352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53809397-C-A

http://identifiers.org/hco/10/GRCh38#110788366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53809410-C-A

110788400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53809443-C-T

110788402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53809445-G-C

110788447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53809490-A-G

110788486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53809529-C-G

110788577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53809612-G-A

110788577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53809612-G-T

110788583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53809617-C-T

110788595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53809629-C-T

http://identifiers.org/hco/10/GRCh38#110788751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53809799-C-A

110789437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53810204-T-C

110789665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53810213-G-A

http://identifiers.org/hco/10/GRCh38#110789886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53810433-C-A

110790051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53810540-G-A

110790408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53810875-T-C

110790409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53810876-A-G

110790658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53811293-A-G

110790705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53811334-G-A

110790705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53811334-G-T

110791090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53811838-C-T

110791131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53811882-T-C

110791169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53811919-T-C

110791438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53812148-C-G

110791574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53812261-C-T

110791738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53812408-G-A

110791996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53812704-G-C

http://identifiers.org/hco/10/GRCh38#110792127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53812814-A-C

110792127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53812814-A-G

110793931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53818030-C-T

110794041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53818141-C-G

110794442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53818537-G-A

110794442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53818537-G-C

110794696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53818744-A-G

110794740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53818783-A-G

110794810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53818845-T-A

110794810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53818845-T-C

110795017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53819043-C-G

110795099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53819128-C-T

110795197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53819209-G-A

110795280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53819278-G-T

110795301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53819292-C-G

110795337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53819326-T-C

110796190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53820166-C-T

110796330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53820335-T-C

http://identifiers.org/hco/10/GRCh38#110796452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53820466-C-A

110796755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53820505-T-A

110796827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53820569-T-A

110797009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53820752-T-G

http://identifiers.org/hco/10/GRCh38#110797072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53820812-A-C

110797401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53820974-G-T

110797421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53820990-G-C

110797421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53820990-G-T

110797457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53821025-G-A

110797511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53821080-G-T

110797537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53821109-G-A

110797576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53821148-G-A

110797576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53821148-G-T

110797724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53821284-A-G

110797743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53821302-T-A

110797743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53821302-T-C

110797798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53821360-G-T

110798024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53821587-G-A

110798068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53821634-T-A

110798769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53822120-T-G

110798785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53822132-A-G

http://identifiers.org/hco/10/GRCh38#110798822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53822181-A-C

110798822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53822181-A-G

110798867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53822215-A-G

110798927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53822277-T-C

110798942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53822289-G-C

110798942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53822289-G-T

110798994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53822337-T-C

http://identifiers.org/hco/10/GRCh38#110799005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53822346-A-C

110799006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53822347-G-C

110799245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53822589-G-A

110799580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53822931-G-A

110799622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53822960-A-G

http://identifiers.org/hco/10/GRCh38#110799657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53822995-C-A

110799657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53822995-C-T

110799702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53823022-A-G

110799710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53823030-G-A

110799710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53823030-G-T

http://identifiers.org/hco/10/GRCh38#110799720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53823040-C-A

110799745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53823056-A-G

110799924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53823216-G-T

http://identifiers.org/hco/10/GRCh38#110799938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53823226-A-C

110799987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53823259-C-T

110800028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53823292-T-A

110800059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53823323-G-A

110800059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53823323-G-T

110800074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53823342-A-G

110800081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53823349-C-G

110800081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53823349-C-T

110800176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53823540-G-A

http://identifiers.org/hco/10/GRCh38#110800202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53823566-A-C

110800415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53824007-G-A

http://identifiers.org/hco/10/GRCh38#110800670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53824223-C-A

110800677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53824230-C-T

110800917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53824430-G-A

110800971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53824493-C-T

110800990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53824516-T-C

110801051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53824570-G-A

110801967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53824833-G-A

110801979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53824845-C-T

110802117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53824981-A-G

http://identifiers.org/hco/10/GRCh38#110802217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53825084-A-C

110802296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53825147-C-G

110802404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53825258-T-A

http://identifiers.org/hco/10/GRCh38#110802463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53825307-C-A

110802463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53825307-C-G

110802463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53825307-C-T

110802686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53825503-T-A

110802742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53825557-G-T

110802961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53825754-T-C

110803048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53825839-T-A

110803048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53825839-T-C

http://identifiers.org/hco/10/GRCh38#110803786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53827183-A-C

http://identifiers.org/hco/10/GRCh38#110803853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53827231-C-A

110803856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53827234-G-A

110803856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53827234-G-T

110803883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53827259-G-A

110803962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53827323-T-C

http://identifiers.org/hco/10/GRCh38#110803974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53827335-C-A

110804214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53827561-G-A

110806710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53827934-G-C

110806737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53827960-T-A

110807826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53828305-T-G

110807827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53828306-G-A

110808527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53828769-T-C

110808550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53828780-G-T

110810228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53829271-C-T

110810270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53829316-G-A

110810272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53829318-A-G

110810299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53829345-A-G

110810439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53829466-G-A

110810439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53829466-G-T

http://identifiers.org/hco/10/GRCh38#110810526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53829546-C-A

110810526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53829546-C-T

http://identifiers.org/hco/10/GRCh38#110810580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53830066-C-A

110810580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53830066-C-T

110810585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53830071-G-A

110810585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53830071-G-T

110810765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53830246-C-T

110810777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53830258-A-G

110810784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53830265-A-G

110810839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53830275-G-A

110810931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53830354-T-C

110811213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53830591-C-T

110811235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53830625-G-T

110811317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53830709-G-A

110811359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53830739-G-A

110811481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53830829-T-C

110811554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53830907-G-A

110811554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53830907-G-T

110811789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53831212-T-C

110811807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53831230-G-A

110811958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53831358-G-A

http://identifiers.org/hco/10/GRCh38#110812133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53831508-C-A

110812133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53831508-C-T

110812136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53831511-T-A

110812136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53831511-T-C

110812136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53831511-T-G

110812145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53831515-G-T

110812154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53831524-G-T

110812168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53831538-A-T

110812184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53831559-A-G

110812232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53831608-T-A

110812232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53831608-T-G

110812332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53831708-G-A

110812332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53831708-G-T

110812396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53831739-G-A

110812396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53831739-G-C

110812396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53831739-G-T

110812452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53831780-G-A

110812455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53831783-A-G

http://identifiers.org/hco/10/GRCh38#110812704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53832032-C-A

110812704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53832032-C-T

http://identifiers.org/hco/10/GRCh38#110812724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53832052-A-C

110812724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53832052-A-G

110812746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53832074-G-C

http://identifiers.org/hco/10/GRCh38#110812785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53832113-C-A

110812785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53832113-C-G

110812785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53832113-C-T

110812790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53832118-C-T

110812822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53832150-C-G

110812822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53832150-C-T

110812833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53832161-T-A

110812845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53832173-G-A

110812845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53832173-G-C

110812914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53832242-T-C

110812914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53832242-T-G

110812961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53832290-T-C

110812961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53832290-T-G

110813010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53832339-A-T

110813032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53832349-T-C

http://identifiers.org/hco/10/GRCh38#110813055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53832370-C-A

110813055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53832370-C-T

110813085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53832400-A-G

110813267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53832570-C-G

110813405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53832704-T-G

110813703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53832954-T-G

110813707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53832958-C-T

110813708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53832959-C-G

110813710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53832961-C-T

110813725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53832976-C-T

110813796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53833036-T-C

http://identifiers.org/hco/10/GRCh38#110813816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53833056-C-A

110813816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53833056-C-T

110814075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53833186-C-T

110814131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53833235-C-T

110814217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53833320-A-G

110814285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53833378-T-C

110814352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53833429-A-G

110814391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53833464-T-C

110814923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53833673-A-G

110815107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53833848-G-A

110815323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53834261-C-T

110815478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53834404-A-G

110816765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53835015-G-T

110817150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53835313-T-A

110817219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53835357-G-A

110818332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53836537-G-T

110818371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53836575-C-T

110818514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53836710-G-C

110818531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53836725-G-A

110818641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53836819-G-T

110819072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53837245-A-G

http://identifiers.org/hco/10/GRCh38#110819894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53838404-A-C

http://identifiers.org/hco/10/GRCh38#110819939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53838436-C-A

110819939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53838436-C-T

110820118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53838561-T-A

110820128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53838571-G-A

110820135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53838578-G-A

110820145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53838588-T-C

http://identifiers.org/hco/10/GRCh38#110820148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53838591-C-A

110820262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53838709-T-G

110820493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53838929-C-T

http://identifiers.org/hco/10/GRCh38#110820661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53839089-C-A

110820909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53839284-T-G

110820986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53839322-A-G

110821096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53839430-G-A

http://identifiers.org/hco/10/GRCh38#110821128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53839459-A-C

110821150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53839481-G-A

110821150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53839481-G-C

110821150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53839481-G-T

110821194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53839527-T-A

110821194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53839527-T-C

http://identifiers.org/hco/10/GRCh38#110821212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53839545-C-A

110821214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53839547-T-C

110821214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53839547-T-G

110821225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53839558-G-C

http://identifiers.org/hco/10/GRCh38#110821458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53839788-C-A

110821458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53839788-C-G

110821458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53839788-C-T

http://identifiers.org/hco/10/GRCh38#110821607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53839934-C-A

110821607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53839934-C-T

110821608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53839935-G-A

110821608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53839935-G-C

110821608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53839935-G-T

110821658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53839985-T-A

110821658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53839985-T-G

110821747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53840074-T-C

110821828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53840155-G-A

110821828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53840155-G-T

110821830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53840157-A-G

110821830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53840157-A-T

http://identifiers.org/hco/10/GRCh38#110821861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53840188-C-A

110821861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53840188-C-G

110821861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53840188-C-T

http://identifiers.org/hco/10/GRCh38#110821985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53840312-C-A

110821993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53840320-A-G

110821993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53840320-A-T

110822108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53840426-C-T

110822252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53840559-A-G

http://identifiers.org/hco/10/GRCh38#110822279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53840600-C-A

110822315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53840633-T-A

110822315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53840633-T-C

110822320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53840638-G-A

110822320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53840638-G-C

110822320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53840638-G-T

110822321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53840639-G-C

110822321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53840639-G-T

110822326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53840644-A-G

110822358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53840684-G-T

110822549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53840897-C-T

http://identifiers.org/hco/10/GRCh38#110822578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53840924-C-A

110822578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53840924-C-G

110822578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53840924-C-T

110822589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53840986-T-C

110823145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53841579-C-T

110823309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53841737-T-C

110823381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53841809-A-T

110823398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53841827-A-G

110823435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53841869-T-A

110823435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53841869-T-C

110823435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron variant
orthologous variants: 53841869-T-G

110823492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense variant
orthologous variants: 53841947-A-T

110823541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: synonymous variant
orthologous variants: 53841996-G-A

110823618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53842070-A-T

http://identifiers.org/hco/10/GRCh38#110823624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53842076-A-C

110823624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53842076-A-G

110823907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53842186-T-G

http://identifiers.org/hco/10/GRCh38#110824193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53842333-C-A

110824321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53842459-C-T

110824337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53842477-A-G

110824381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53842520-G-A

110824903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53842865-T-C

110824903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53842865-T-G

110827484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53844890-G-A

http://identifiers.org/hco/10/GRCh38#110827622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53845013-C-A

110827653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53845041-T-C

110827659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53845047-G-A

110827659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53845047-G-T

110827690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53845070-T-C

110827772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53845149-C-T

110827816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53845192-G-T

110827825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53845201-G-C

110827888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53845259-A-G

110827889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53845260-A-G

110827890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53845261-G-A

110827912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53845283-G-A

110827912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53845283-G-T

110827943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53845314-G-A

110827943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53845314-G-T

110828067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53845414-C-G

110828067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53845414-C-T

110828222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53845574-T-C

110828387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53845721-G-A

110828659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53845975-C-T

110828994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53846259-C-G

110829199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53846442-G-A

110829237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53846483-G-T

110829521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53846754-A-G

110830505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53847294-C-G

110830505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53847294-C-T

110830559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53847348-G-A

http://identifiers.org/hco/10/GRCh38#110830603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53847393-C-A

110830603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53847393-C-T

110830889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53847656-G-A

110830917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53847689-G-A

110830917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53847689-G-C

http://identifiers.org/hco/10/GRCh38#110830948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53847716-C-A

110830948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53847716-C-T

110830959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53847733-T-G

http://identifiers.org/hco/10/GRCh38#110831025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53847787-C-A

110831162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53847924-G-C

110831173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53847935-G-C

110831213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53847975-C-T

110831226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53847989-G-A

110831226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53847989-G-T

http://identifiers.org/hco/10/GRCh38#110831352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53848102-C-A

110831404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53848153-T-C

110831404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53848153-T-G

http://identifiers.org/hco/10/GRCh38#110831433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53848182-C-A

110831439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53848188-G-A

110831467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53848196-T-A

110831467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53848196-T-C

110831496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53848225-G-T

http://identifiers.org/hco/10/GRCh38#110831520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53848249-C-A

http://identifiers.org/hco/10/GRCh38#110831521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53848250-A-C

110831521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53848250-A-G

http://identifiers.org/hco/10/GRCh38#110831566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53848277-C-A

110831566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53848277-C-T

110831577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53848288-G-T

110831640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53848340-T-A

110831762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53848452-A-G

110831876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53848555-A-G

110831938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53848622-G-A

110831991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53848769-G-A

http://identifiers.org/hco/10/GRCh38#110832016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53848794-A-C

110832081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53848841-A-G

110832110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53848981-A-G

110832903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53850053-T-C

110832934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53850084-A-G

110833654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53850521-C-T

http://identifiers.org/hco/10/GRCh38#110833867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53850791-A-C

110833922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53850890-A-G

110834246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851180-G-C

110834289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851223-G-C

110834305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851240-C-G

110834305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851240-C-T

110834549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851417-A-G

110834629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851517-T-C

110834797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851659-T-G

110834874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851720-A-G

http://identifiers.org/hco/10/GRCh38#110835075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53851907-C-A

110835075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851907-C-G

110835075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851907-C-T

110835100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851916-A-G

110835182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53851967-T-C

http://identifiers.org/hco/10/GRCh38#110835248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53852032-C-A

110835248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53852032-C-T

110835791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53852427-G-A

110835791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53852427-G-T

http://identifiers.org/hco/10/GRCh38#110835813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53852454-C-A

http://identifiers.org/hco/10/GRCh38#110835844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53852482-C-A

110835852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53852490-C-G

110835879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53852522-C-T

110835933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53852576-A-G

110835933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53852576-A-T

http://identifiers.org/hco/10/GRCh38#110835939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53852582-C-A

110835939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53852582-C-T

http://identifiers.org/hco/10/GRCh38#110835940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53852583-A-C

110835940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53852583-A-G

http://identifiers.org/hco/10/GRCh38#110835993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53852627-C-A

110835993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53852627-C-T

http://identifiers.org/hco/10/GRCh38#110836158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53852772-A-C

110836158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53852772-A-G

110836173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53852789-T-C

http://identifiers.org/hco/10/GRCh38#110836182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53852798-C-A

110836182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53852798-C-T

110836212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53852823-T-C

110836274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53852864-C-T

http://identifiers.org/hco/10/GRCh38#110836283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53852873-C-A

110836373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53852962-A-G

110836378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53852967-T-A

110836378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53852967-T-G

110836452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53853040-G-A

110836539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53853112-G-A

110836539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53853112-G-T

http://identifiers.org/hco/10/GRCh38#110836569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53853142-C-A

110836569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53853142-C-T

http://identifiers.org/hco/10/GRCh38#110836571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53853143-C-A

110836608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53853467-T-G

http://identifiers.org/hco/10/GRCh38#110836632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53853495-C-A

http://identifiers.org/hco/10/GRCh38#110836652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53853516-C-A

110836652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53853516-C-T

110836796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53853700-A-G

110837182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53853985-A-G

http://identifiers.org/hco/10/GRCh38#110837240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53854030-C-A

110837240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53854030-C-T

110837289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53854067-T-C

110837408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53854176-G-T

110837635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53854333-T-C

110837652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53854350-G-T

http://identifiers.org/hco/10/GRCh38#110837746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53854451-C-A

110837746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53854451-C-T

http://identifiers.org/hco/10/GRCh38#110837771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53854476-C-A

http://identifiers.org/hco/10/GRCh38#110838535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53854673-C-A

110838553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53854682-T-C

http://identifiers.org/hco/10/GRCh38#110838573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53854696-A-C

http://identifiers.org/hco/10/GRCh38#110838635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53854754-A-C

110838635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53854754-A-G

http://identifiers.org/hco/10/GRCh38#110838637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53854756-C-A

110838637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53854756-C-T

110838677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53854774-T-A

110838700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53854805-T-G

110838758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53854851-G-T

http://identifiers.org/hco/10/GRCh38#110838844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53854922-C-A

110838844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53854922-C-T

110838888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27424
most severe consequence: 3 prime UTR variant
orthologous variants: 53854958-C-T