36306628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156455829-G-T

http://identifiers.org/hco/20/GRCh38#36306656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156455842-C-A

36306847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156455967-C-T

36306941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156456030-T-A

http://identifiers.org/hco/20/GRCh38#36307062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156456094-C-A

36307166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156456186-G-T

36307967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156456896-T-G

36308599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156457500-T-A

36308876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156457779-G-T

36309144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156458036-T-G

36309187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156458079-C-T

36309195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156458086-G-A

36309588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156458462-G-A

36309841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156458676-A-G

36309867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156458701-G-A

36309882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156458715-T-A

36309929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156458748-G-A

36310003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156458821-G-A

36310321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156458902-C-T

36310356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156458934-C-T

36311079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156459388-C-T

36311120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156459429-C-T

36311177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156459487-G-C

36311223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156459523-A-G

36311259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156459548-C-T

36311398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156459681-G-A

36311398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156459681-G-T

36311409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156459692-C-T

36311410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156459693-G-A

36311410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156459693-G-C

36311466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156459749-C-T

36311825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156460101-C-G

36311825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156460101-C-T

http://identifiers.org/hco/20/GRCh38#36311836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156460112-C-A

36311836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156460112-C-T

36311837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156460113-G-A

36311837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156460113-G-T

36311862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156460138-G-C

36312032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156460306-T-A

36312885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156460894-T-C

36312933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156460915-C-G

http://identifiers.org/hco/20/GRCh38#36313174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156461157-C-A

36313236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156461220-C-T

36313774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156461676-T-C

36313862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156461757-C-T

http://identifiers.org/hco/20/GRCh38#36313864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156461759-C-A

36314016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156461820-G-A

36314357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156462152-G-A

36314846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156462379-T-A

36314939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156462460-C-G

36314939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156462460-C-T

36315004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156462565-G-C

36315037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156462607-T-G

36315268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156463008-C-T

36315402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156463148-C-T

36315530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156463271-G-T

36315697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156463449-C-T

36315815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156463564-T-C

36316179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156463895-C-T

36320565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156466473-A-G

36320713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156466615-C-T

36320869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156466769-G-A

36320921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156466815-G-C

http://identifiers.org/hco/20/GRCh38#36320924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156466818-C-A

36320975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156466854-G-A

http://identifiers.org/hco/20/GRCh38#36321191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156467050-C-A

36321309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156467169-A-G

36321425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156467282-G-A

36321428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156467285-A-G

36321494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156467349-C-T

36321671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156467515-C-T

36322121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156467875-T-C

36322231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156467980-G-A

36322246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156467995-T-C

36322460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156468116-A-G

36327359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156481103-T-G

36328423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156481516-A-G

http://identifiers.org/hco/20/GRCh38#36331026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156482618-A-C

36331181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156482734-C-G

36331363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156482861-T-G

36331373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156482869-C-T

36331458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156482926-C-T

36331553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156482999-G-C

36331595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156483042-C-T

36333268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156485483-G-A

36333688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156486024-G-A

36333901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156486270-G-A

36333987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156486343-G-C

36334186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156486545-A-G

36334483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156486776-C-T

36334492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156486785-C-G

36334608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156486886-G-T

36334612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156486890-G-A

36335130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156487288-C-G

36335172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156487324-T-C

36335344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156487441-C-T

36335562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156487594-G-A

36335580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156487612-G-A

36335580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156487612-G-T

36335636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156487660-T-G

http://identifiers.org/hco/20/GRCh38#36335892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156487808-C-A

36335892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156487808-C-G

36335965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156487904-C-G

36335965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156487904-C-T

36335966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156487905-G-A

36335966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156487905-G-C

36336018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156487967-A-G

36336224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156488169-G-A

36336554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156488341-A-T

36336581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156488368-T-C

36336864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156488624-C-T

36336881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156488641-C-G

36337172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156489182-C-T

36337401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156489420-A-G

36337450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156489466-C-T

http://identifiers.org/hco/20/GRCh38#36337500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156489529-C-A

36337725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156489731-C-T

36337935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156489901-G-A

36338082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156490027-T-G

36338083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156490028-C-G

36338176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156490124-C-T

36338206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156490154-A-T

36340222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156491030-C-G

36340222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156491030-C-T

http://identifiers.org/hco/20/GRCh38#36340260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156491069-C-A

36340260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156491069-C-T

36340327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156491114-G-A

http://identifiers.org/hco/20/GRCh38#36340987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156491700-C-A

36341017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156491727-C-T

36341063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156491768-C-T

36341169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156491849-C-T

36341370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156492032-C-G

36341405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156492064-C-T

http://identifiers.org/hco/20/GRCh38#36341411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156492069-C-A

36341480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156492094-G-A

36341480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156492094-G-T

36341532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156492144-C-T

36341621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156492230-G-T

36341935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156492498-A-G

36342362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156492903-G-A

36342757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156493323-G-A

http://identifiers.org/hco/20/GRCh38#36342774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156493345-C-A

36342861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156493414-G-A

36342861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156493414-G-C

36342861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156493414-G-T

36342926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156493481-G-A

36342926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156493481-G-C

36343052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156493594-G-A

36343054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156493596-G-A

36343237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156493761-C-T

http://identifiers.org/hco/20/GRCh38#36344037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156494451-C-A

36344089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156494486-C-T

36344138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156494534-A-T

36344624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, undefined
orthologous variants: 156494882-C-G

36344624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, undefined
orthologous variants: 156494882-C-T

36344648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, undefined
orthologous variants: 156494904-T-C

36344766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, undefined
orthologous variants: 156494980-G-A

36345006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, undefined
orthologous variants: 156495212-C-T

36345042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, undefined
orthologous variants: 156495244-C-T

http://identifiers.org/hco/20/GRCh38#36345091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156495274-C-A

36345138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156495321-G-A

36345417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156495576-T-C

36345480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156495629-G-A

36345610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156495733-C-T

36346323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156496093-G-A

36346439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156496196-G-A

36347302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156496977-G-A

36347379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156497039-C-T

36347400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156497053-C-T

36347466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156497117-G-C

36354020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156497482-C-T

36354116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156497557-A-G

36354187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156497615-C-T

36354220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156497648-C-T

36359451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156500278-G-A

36359565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156500386-G-A

36359628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156500443-G-A

36359690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156500491-G-A

36359779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156500575-G-A

36360143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156501257-C-G

36360163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156501277-T-A

36360363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156501444-C-G

http://identifiers.org/hco/20/GRCh38#36360524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156501578-A-C

36360605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156501643-T-C

36360730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156501791-G-A

http://identifiers.org/hco/20/GRCh38#36360734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156501795-C-A

36360748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156501810-G-A

http://identifiers.org/hco/20/GRCh38#36360916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156501972-A-C

36361558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156502446-C-T

36361641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156502513-G-A

36365802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156505809-C-G

36365802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156505809-C-T

36365807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156505812-G-A

36365927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156505920-A-T

36366637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156506312-A-T

http://identifiers.org/hco/20/GRCh38#36366947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156506632-C-A

36366947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156506632-C-T

36366979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156506659-T-C

http://identifiers.org/hco/20/GRCh38#36366986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156506666-C-A

http://identifiers.org/hco/20/GRCh38#36367049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156506723-C-A

36367049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5 prime UTR variant
orthologous variants: 156506723-C-T

36367154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5 prime UTR variant
orthologous variants: 156506787-C-T

36367238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5 prime UTR variant
orthologous variants: 156506870-A-G

36367246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5 prime UTR variant
orthologous variants: 156506878-G-A

36367246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5 prime UTR variant
orthologous variants: 156506878-G-T

http://identifiers.org/hco/20/GRCh38#36367287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156506911-C-A

36367287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156506911-C-T

36367296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156506920-G-A

http://identifiers.org/hco/20/GRCh38#36367345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156506968-C-A

36367345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156506968-C-T

36367534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156507153-G-A

36368148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156507627-A-G

http://identifiers.org/hco/20/GRCh38#36368213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156507668-C-A

36368738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156508155-A-G

36368747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156508165-G-T

36368827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156508245-G-A

36370045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156509413-C-T

36370177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156509542-G-C

36371313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156510309-A-G

36371895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156510756-C-T

36372142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156510899-G-A

36372250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156510989-C-T

36372256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156511000-G-A

36372263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156511007-G-A

36372384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156511119-C-T

36372448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156511179-C-T

http://identifiers.org/hco/20/GRCh38#36372550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156511255-C-A

36372956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156512030-C-T

36372957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156512031-A-G

36373181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156512234-C-T

36373345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156512375-A-G

36373466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156512478-C-G

36373698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156512659-T-G

36373989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156512984-A-T

36374020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156513014-G-A

36374020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156513014-G-C

36374061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156513049-T-A

36374061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156513049-T-G

36374399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156513348-T-C

36374810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156513729-T-C

36374882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156513804-A-T

36374922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156513842-A-G

36375020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156513937-T-C

36375030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156513947-G-A

36375191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156514098-T-C

http://identifiers.org/hco/20/GRCh38#36375308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156514221-A-C

36375319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156514232-G-A

36375404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156514265-C-T

36375426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156514287-C-T

36375616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156514470-G-A

36377029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156514779-A-G

36377372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156515054-T-G

36378063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156515651-C-T

36378104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156515698-G-A

36378273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156515869-G-A

36378393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156515985-T-C

36378413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156516000-C-T

36378606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156516149-A-G

36378945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156516446-T-C

36378962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156516462-C-T

36379160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156516610-A-G

36379161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156516611-C-T

36379288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156516717-G-A

36379288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156516717-G-T

36379581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156516904-A-T

36379645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156516962-C-T

36380000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156517318-A-G

36383314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156518278-A-G

36383346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156518308-T-C

36383352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156518311-A-G

36384011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156518834-G-A

36384336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, undefined
orthologous variants: 156519172-G-A

36384454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156519286-A-G

36384989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156519614-G-A

http://identifiers.org/hco/20/GRCh38#36385021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156519663-C-A

36385294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156519894-G-A

36385356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156519952-G-T

36385368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156519964-A-T

36385446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156520005-C-T

36385551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156520100-A-G

36386006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156520529-A-G

36386057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156520586-G-A

36386058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156520587-G-A

36386383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156520861-G-A

36389606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156522967-C-T

36389697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156523061-A-G

36389881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156523237-T-C

http://identifiers.org/hco/20/GRCh38#36390396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156523661-C-A

36390396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156523661-C-T

36390466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156523725-G-A

36390499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156523758-G-C

36390645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156523886-G-A

36390645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156523886-G-C

36391083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156524547-A-G

36391282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156524731-C-T

36391404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156524843-C-T

http://identifiers.org/hco/20/GRCh38#36391698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156525115-C-A

36391698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156525115-C-T

36393042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156526633-G-A

36393304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156526868-C-T

36393305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156526869-A-G

36393339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156526887-T-C

http://identifiers.org/hco/20/GRCh38#36393346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156526894-C-A

36393554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156527033-C-T

36393742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156527189-T-C

36393743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156527190-G-T

36393787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156527231-G-A

36393866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156527296-C-T

36394097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156527499-C-T

http://identifiers.org/hco/20/GRCh38#36394099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156527501-C-A

36394099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156527501-C-T

36394598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, undefined
orthologous variants: 156528164-G-A

36394626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156528192-G-A

36394697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156528262-C-T

36394735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156528300-T-C

36394861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, undefined
orthologous variants: 156528426-G-A

36394861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, undefined
orthologous variants: 156528426-G-C

http://identifiers.org/hco/20/GRCh38#36395055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156528580-C-A

36396102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156529093-G-A

36398610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156530676-A-G

http://identifiers.org/hco/20/GRCh38#36398644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156530705-A-C

36398651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156530712-T-C

36400684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156530975-G-A

36400758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156531040-G-C

36400758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156531040-G-T

36400903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156531115-G-A

36400919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156531131-G-A

36400974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156531171-A-G

36401078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156531241-G-A

36401078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156531241-G-C

36401078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156531241-G-T

36401083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156531246-G-C

36401170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156531315-G-A

http://identifiers.org/hco/20/GRCh38#36401255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#156531397-C-A

36401255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, undefined
orthologous variants: 156531397-C-T

36401549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156531638-A-G

36401788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156531823-G-C

36401919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156531956-T-A

36411983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156533775-G-A

36412159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156533940-G-T

36412303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156534069-G-A

36412324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156534086-C-G

36412468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156534215-G-A

36412468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156534215-G-T

36412771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156534477-G-A

36412771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156534477-G-C

36418606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156536660-G-A

36418790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156536820-C-T

36418873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156536900-G-A

36419020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156537016-G-A

36421556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156538262-C-T

36421605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156538309-A-G

36421618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156538322-A-G

36421909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156538519-G-A

36421978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156538574-G-A

36422254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156538767-A-T

36422434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156538963-G-A

36422519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156539043-C-T

36422588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156539110-G-T

36422596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156539118-T-G

36423065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156539558-C-T

36423121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156539591-G-A

http://identifiers.org/hco/20/GRCh38#36430087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156541562-C-A

36430205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156541696-C-T

36430325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156541818-T-C

36431520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156542406-A-G

36431521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156542407-G-T

http://identifiers.org/hco/20/GRCh38#36431523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156542409-C-A

http://identifiers.org/hco/20/GRCh38#36431527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156542413-C-A

36431572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156542445-G-T

http://identifiers.org/hco/20/GRCh38#36431590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156542467-A-C

36431595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156542472-T-C

36431617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156542497-G-A

36431617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156542497-G-T

36431792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: synonymous variant
orthologous variants: 156542673-A-G

36431828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: synonymous variant
orthologous variants: 156542709-G-A

36431975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: synonymous variant
orthologous variants: 156542856-C-T

36431990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: missense variant
orthologous variants: 156542871-T-A

36431990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: synonymous variant
orthologous variants: 156542871-T-C

36432418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: missense variant
orthologous variants: 156543296-C-T

36432762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156543979-G-A

36432762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156543979-G-T

36432923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156544149-C-T

http://identifiers.org/hco/20/GRCh38#36433111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156544332-C-A

36433300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156544480-C-T

36433367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156544534-G-C

36434622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156545133-C-G

36434792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156545266-G-A

36434792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156545266-G-C

36435045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156545447-G-T

http://identifiers.org/hco/20/GRCh38#36435187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156545586-A-C

36435489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156545794-G-A

36435675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156545885-C-T

36435964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156546183-G-A

36435964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156546183-G-T

36436040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156546231-G-A

36436040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156546231-G-C

36436040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156546231-G-T

http://identifiers.org/hco/20/GRCh38#36436056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156546247-C-A

http://identifiers.org/hco/20/GRCh38#36436114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156546335-C-A

36436114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: synonymous variant
orthologous variants: 156546335-C-G

36436114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: synonymous variant
orthologous variants: 156546335-C-T

36436147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: synonymous variant
orthologous variants: 156546368-G-A

36436147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: synonymous variant
orthologous variants: 156546368-G-T

36436267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: synonymous variant
orthologous variants: 156546491-G-A

36436267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: missense variant
orthologous variants: 156546491-G-C

36436267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: missense variant
orthologous variants: 156546491-G-T

36436288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: synonymous variant
orthologous variants: 156546512-G-T

36436312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: synonymous variant
orthologous variants: 156546536-C-G

36436348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 156546572-C-G

http://identifiers.org/hco/20/GRCh38#36436349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156546573-A-C

36436349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 156546573-A-G

http://identifiers.org/hco/20/GRCh38#36436408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156546627-A-C

36436408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156546627-A-G

36436432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156546651-T-A

36436432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156546651-T-G

36436433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156546652-G-A

36436433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156546652-G-T

36437014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156546788-C-G

36437032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156546806-C-T

36437034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156546808-C-T

36437085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156546858-A-G

36437092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156546870-G-C

36437097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156546875-A-G

36437250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156546958-C-G

36439170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156547142-C-T

36439186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156547158-G-A

36439567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156547496-G-C

http://identifiers.org/hco/20/GRCh38#36439615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#156547539-A-C

36439615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, undefined
orthologous variants: 156547539-A-G

36439615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, undefined
orthologous variants: 156547539-A-T

36439647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156547571-G-A

36439647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156547571-G-T

36439659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156547583-T-C

36439659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156547583-T-G

36439899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156547914-G-A

36439899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156547914-G-C

36439899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156547914-G-T

http://identifiers.org/hco/20/GRCh38#36441404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156547982-C-A

36441411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156547989-A-G

36441515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156548087-C-T

36441534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156548108-C-G

36441793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156548363-G-A

36441887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156548432-C-T

36442009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156548462-C-G

36442589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156548903-T-C

36442620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156548930-A-G

http://identifiers.org/hco/20/GRCh38#36442724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156548995-C-A

36442724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 156548995-C-T

36443281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156549655-C-T

36443387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156549759-G-T

http://identifiers.org/hco/20/GRCh38#36445648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156551420-A-C

36445668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156551439-T-C

36445678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156551449-G-T

36446708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: synonymous variant
orthologous variants: 156552952-A-G

36446759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: synonymous variant
orthologous variants: 156553003-G-A

36446769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: missense variant
orthologous variants: 156553013-G-A

36446792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: synonymous variant
orthologous variants: 156553036-A-G

36446804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: synonymous variant
orthologous variants: 156553048-C-T

http://identifiers.org/hco/20/GRCh38#36446976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156553220-C-A

36446976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156553220-C-T

http://identifiers.org/hco/20/GRCh38#36446986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156553230-C-A

36446986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156553230-C-T

http://identifiers.org/hco/20/GRCh38#36446999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156553243-C-A

36447004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156553248-G-A

36447026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156553269-G-A

36447026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156553269-G-T

36447029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156553272-G-A

36447029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156553272-G-T

36447036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156553279-G-A

36447190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156553370-C-T

36447335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156553513-G-T

36449301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156554470-T-C

36449385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156554541-G-A

36449640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156554749-T-C

36449760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156554983-G-T

36449962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156555139-G-T

36450115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156555283-C-T

36454412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156559059-C-G

36454828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, undefined
orthologous variants: 156559361-C-T

http://identifiers.org/hco/20/GRCh38#36455172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156559644-A-C

36455172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156559644-A-G

36455301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156559720-C-G

36455301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156559720-C-T

http://identifiers.org/hco/20/GRCh38#36455494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156559976-C-A

36455787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156560256-C-T

36455852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156560293-A-G

36455856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156560297-T-C

36455880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156560315-C-T

36455925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156560364-T-C

36459109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron variant
orthologous variants: 156561685-G-A

http://identifiers.org/hco/20/GRCh38#36461372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#156562878-C-A

36461372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 156562878-C-T

36461495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 156562992-T-C

http://identifiers.org/hco/20/GRCh38#36461580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156563086-C-A

36461580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156563086-C-T

36461606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 156563121-G-A

36461606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 156563121-G-T

http://identifiers.org/hco/20/GRCh38#36461898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156563366-C-A

http://identifiers.org/hco/20/GRCh38#36462107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156563568-C-A

http://identifiers.org/hco/20/GRCh38#36462355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#156563803-C-A

36462355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 156563803-C-T

36462441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156563868-G-A

36462441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156563868-G-C

36462441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156563868-G-T

36463241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156564660-G-A

36464099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156565790-G-A

36464118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156565809-G-A

36464572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156566129-G-A

36465134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156566563-A-G

36465200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156566613-G-T

36465355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156566759-C-G

36465355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156566759-C-T

36465401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156566804-A-T

36465403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156566806-G-A

36465403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156566806-G-T

http://identifiers.org/hco/20/GRCh38#36465451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156566847-C-A

36465474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156566871-G-A

36465474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156566871-G-T

36465525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156566921-C-T

36465924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156567306-C-T

36466690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156568014-T-C

36466702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156568026-A-G

36466899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156568184-G-A

http://identifiers.org/hco/20/GRCh38#36467072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156568236-C-A

36467159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156568323-A-T

36467226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156568390-T-C

36467654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156568815-A-G

36467764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 156568887-G-A

36467947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 156569070-C-T

36468071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156569242-A-G

36468311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156569439-C-T

36468317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156569445-C-T

36468673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 156569728-T-C

36468686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156569746-A-T

36468787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156569884-G-A

36468929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156569997-A-G

36469861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156570611-G-A

36469902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156570656-G-C

36470221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156570962-A-G

36470253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156570993-G-A

36470303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156571059-C-T

36470304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156571060-C-T

36471788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156572162-G-A

36471806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156572180-A-T

36472106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156572381-C-T

36473013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 156572818-A-T

36473077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 156572895-G-A

36473077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 156572895-G-T

36473188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156572992-C-T

36473264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156573055-C-T

36473331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156573095-T-A

36473730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156573379-G-A

36473741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156573390-T-C

36473820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156573439-G-A

36473827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156573446-C-T

36473841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156573460-A-G

36474227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156573810-G-A

36474227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156573810-G-C

36474319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156573926-C-G

36474498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156574073-T-C

36474770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156574359-G-C

36474907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156574481-C-T

36477064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156576263-T-C

36478252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156577047-C-T

36478261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156577056-T-C

36478458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156577243-C-T

36478680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156577410-G-A

36479089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156577635-A-T

36481929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156578829-G-A

36481929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156578829-G-T

36481937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156578837-G-A

36482004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156578897-T-C

36482031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156578921-C-G

36482108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156578971-T-C

36482139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156578999-A-G

http://identifiers.org/hco/20/GRCh38#36482160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156579012-A-C

36482160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156579012-A-T

http://identifiers.org/hco/20/GRCh38#36482172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156579023-A-C

36482237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156579086-G-T

36482322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156579172-T-C

36482411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156579244-A-G

http://identifiers.org/hco/20/GRCh38#36487248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156580057-C-A

36487270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156580079-C-T

http://identifiers.org/hco/20/GRCh38#36487490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156580249-C-A

36487505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156580257-C-T

36487581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156580320-A-G

36487597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156580336-C-G

36487691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156580362-C-G

36487705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156580368-C-T

36488877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156581038-A-T

36489109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156581227-G-A

36489193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156581308-C-T

36489257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156581384-T-C

36489264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156581391-A-G

36489648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156581650-G-A

36490150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156581885-G-A

36490398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156582083-A-G

36490790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156582416-G-A

36490816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156582442-C-T

36491797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 156584040-A-G

36492318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156584350-A-G

36492431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156584433-T-C

36492435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156584437-T-C

http://identifiers.org/hco/20/GRCh38#36492551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156584520-C-A

36492551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156584520-C-T

http://identifiers.org/hco/20/GRCh38#36492657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156584596-C-A

36492810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156584708-G-C

http://identifiers.org/hco/20/GRCh38#36492811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156584709-A-C

http://identifiers.org/hco/20/GRCh38#36492819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156584717-C-A

36492842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156584741-C-T

36492894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156584788-T-C

http://identifiers.org/hco/20/GRCh38#36492932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156584830-A-C

36492957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156584853-A-G

http://identifiers.org/hco/20/GRCh38#36492999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156584878-C-A

36492999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156584878-C-T

36493093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156584938-G-A

36493093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156584938-G-T

36493186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 156585006-G-T

http://identifiers.org/hco/20/GRCh38#36493239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#156585039-C-A

36493239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 156585039-C-T

http://identifiers.org/hco/20/GRCh38#36493321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156585093-C-A

36493337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156585110-C-T

36493572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156585313-G-C

36493642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156585357-G-A

36493833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156585539-C-T

36493910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156585603-C-G

36493910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156585603-C-T

36493963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156585647-G-A

36494054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156585728-T-C

36494821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156586519-A-G

36495012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156586708-G-A

36495012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156586708-G-T

36495032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156586717-G-T

36495223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156586841-C-G

36495606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156587188-G-A

36495633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156587205-C-T

36495772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156587319-G-A

36496301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156587481-G-A

36496301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156587481-G-T

http://identifiers.org/hco/20/GRCh38#36496559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156587650-C-A

36496576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156587665-T-C

36496657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156587718-G-A

36496696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156587746-C-G

36496696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156587746-C-T

36496772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156587822-G-A

36497396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156588424-G-A

36497396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156588424-G-T

36497461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156588488-G-A

36497461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156588488-G-C

36497652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156588675-G-A

36497675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156588697-A-T

36497680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156588702-G-T

36497763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156588772-A-G

36497807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156588803-G-A

36497807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156588803-G-T

http://identifiers.org/hco/20/GRCh38#36497809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156588805-C-A

36497809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156588805-C-T

http://identifiers.org/hco/20/GRCh38#36497820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156588816-C-A

36497820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156588816-C-T

36497856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156588854-T-C

36497923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156588919-A-G

36498027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156589020-G-A

http://identifiers.org/hco/20/GRCh38#36498029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156589022-C-A

36498029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156589022-C-T

http://identifiers.org/hco/20/GRCh38#36498055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156589039-C-A

36498119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156589090-G-T

http://identifiers.org/hco/20/GRCh38#36498219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156589138-C-A

36498219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156589138-C-T

36498233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156589152-C-G

http://identifiers.org/hco/20/GRCh38#36498374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156589283-C-A

36498374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156589283-C-T

36498426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156589328-C-T

http://identifiers.org/hco/20/GRCh38#36498461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156589367-C-A

36498471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156589377-T-C

http://identifiers.org/hco/20/GRCh38#36498474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156589380-C-A

http://identifiers.org/hco/20/GRCh38#36498522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156589428-C-A

36498522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156589428-C-T

http://identifiers.org/hco/20/GRCh38#36498573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156589465-C-A

36498646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156589496-T-C

http://identifiers.org/hco/20/GRCh38#36498771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156589606-C-A

36498776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156589610-T-G

36499118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156589840-T-A

36499293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156589994-G-A

36499654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156590318-G-A

36499654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156590318-G-T

http://identifiers.org/hco/20/GRCh38#36500406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156591071-C-A

36500406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 156591071-C-T

http://identifiers.org/hco/20/GRCh38#36500420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156591085-C-A

36500420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156591085-C-T

36500550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156591215-G-A

36500623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156591288-A-G

36500726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156591347-G-T

36500727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156591348-G-A

36500727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156591348-G-T

36500728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156591349-G-A

36500728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156591349-G-T

36501553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156591860-C-G

36501971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156592273-T-G

36501978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156592280-T-C

http://identifiers.org/hco/20/GRCh38#36524211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156602735-C-A

http://identifiers.org/hco/20/GRCh38#36524427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156602947-C-A

36524427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156602947-C-G

36524427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156602947-C-T

36524453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156602967-G-A

36524453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156602967-G-T

http://identifiers.org/hco/20/GRCh38#36524482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156602996-C-A

36524482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156602996-C-T

36524521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156603031-G-A

36524536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156603045-C-T

36524603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156603102-A-G

36525508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156603372-T-A

36525508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156603372-T-C

36525508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156603372-T-G

http://identifiers.org/hco/20/GRCh38#36525542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156603407-A-C

http://identifiers.org/hco/20/GRCh38#36525572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156603435-A-C

36525572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 156603435-A-G

36525663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156603534-C-G

36525663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156603534-C-T

36525793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156603637-G-A

36525793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156603637-G-C

36525793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156603637-G-T

36526194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156604032-T-C

36526201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156604039-G-A

36526201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156604039-G-C

36526201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156604039-G-T

36526422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156604243-C-T

36526745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156604537-G-T

36526953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 156604745-T-C

36527036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156604828-A-G

36527166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156604949-T-A

36527166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156604949-T-C

http://identifiers.org/hco/20/GRCh38#36527203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156604986-C-A

36527203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156604986-C-T

36527242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156605028-A-G

36527242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156605028-A-T

36527322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156605106-C-T

36527400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156605181-G-A

36527400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156605181-G-T

http://identifiers.org/hco/20/GRCh38#36527779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156605492-C-A

36527779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156605492-C-T

http://identifiers.org/hco/20/GRCh38#36527888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156605577-C-A

36527888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156605577-C-T

36527894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156605583-T-C

36528137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156605817-T-C

36528186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156605837-G-A

36528186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156605837-G-C

36528186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156605837-G-T

36528261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156605904-C-T

36528314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156605957-G-A

36528314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156605957-G-T

36528350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156606007-G-A

36528350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156606007-G-T

36528351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156606008-A-G

http://identifiers.org/hco/20/GRCh38#36528366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#156606024-C-A

36528401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156606059-T-C