Variant #0000998531 (NC_000010.10:g.79397387_79397388insTGC, NM_001014797.2:c.15_16insAGC (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.79397387_79397388insTGC
DNA change (hg38) -
Published as KCNMA1(NM_001161352.1):c.15_16insAGC (p.(Gly5_Gly6insSer)), KCNMA1(NM_001322830.1):c.15_16insAGC (p.G5_G6insS)
ISCN -
DB-ID KCNMA1_000096 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
KCNMA1 NM_001014797.2 -?/. - c.15_16insAGC r.(?) p.(Gly5_Gly6insSer)


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