Variant #0001037292 (NC_000009.11:g.138590310C>T, NM_020822.2:c.-3795C>T (KCNT1))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.138590310C>T
DNA change (hg38) -
Published as SOHLH1(NM_001101677.2):c.210G>A (p.(Ser70=))
ISCN -
DB-ID KCNT1_000263
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00421 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SOHLH1 NM_001012415.2 -?/. - c.210G>A r.(?) p.(=)
KCNT1 NM_020822.2 -?/. - c.-3795C>T r.(?) p.(=)


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