All variants in the KCNT1 gene

Information The variants shown are described using the NM_020822.2 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-?/. - c.333G>A r.(?) p.(Ser111=) - likely benign g.138642022G>A g.135750176G>A KCNT1(NM_020822.2):c.333G>A (p.S111=) - KCNT1_000025 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Groningen
-?/. - c.333G>A r.(?) p.(Ser111=) - likely benign g.138642022G>A g.135750176G>A KCNT1(NM_020822.2):c.333G>A (p.S111=) - KCNT1_000025 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Utrecht
-?/. - c.333G>A r.(?) p.(Ser111=) - likely benign g.138642022G>A - KCNT1(NM_020822.2):c.333G>A (p.S111=) - KCNT1_000025 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
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