Variant #0000541038 (NC_000010.10:g.79397359_79397388del, NM_001014797.2:c.27_56del (KCNMA1))

Chromosome 10
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.79397359_79397388del
DNA change (hg38) g.77637601_77637630del
Published as KCNMA1(NM_002247.4):c.27_56delCGGCAGCAGCGGCGGCGGCGGCGGCGGCGG (p.G13_S22del)
ISCN -
DB-ID KCNMA1_000095
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCNMA1 NM_001014797.2 ?/. - c.27_56del r.(?) p.(Gly13_Ser22del)


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