Variant #0000541028 (NC_000010.10:g.78850253G>A, NM_001014797.2:c.1239C>T (KCNMA1))

Chromosome 10
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.78850253G>A
DNA change (hg38) g.77090495G>A
Published as KCNMA1(NM_001014797.3):c.1239C>T (p.C413=), KCNMA1(NM_001322830.1):c.1239C>T (p.C413=)
ISCN -
DB-ID KCNMA1_000085 See all 2 reported entries
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) 3.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCNMA1 NM_001014797.2 -?/. - c.1239C>T r.(?) p.(Cys413=)


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