Variant #0000690794 (NC_000010.10:g.79397361_79397366dup, NM_001014797.2:c.51_56dup (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.79397361_79397366dup
DNA change (hg38) -
Published as KCNMA1(NM_001161352.1):c.51_56dupCGGCGG (p.(Gly18_Gly19dup)), KCNMA1(NM_002247.4):c.51_56dupCGGCGG (p.G19_G20dup)
ISCN -
DB-ID KCNMA1_000058 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCNMA1 NM_001014797.2 ?/. - c.51_56dup r.(?) p.(Gly19_Gly20dup)


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