Variant #0001065262 (NC_000010.10:g.75599312C>T, NM_172169.2:c.994G>A (CAMK2G))

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.75599312C>T
DNA change (hg38) -
Published as CAMK2G(NM_001367534.1):c.994G>A (p.(Gly332Ser))
ISCN -
DB-ID CAMK2G_000023
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 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CAMK2G NM_001367543.1 -?/. - c.994G>A r.(?) p.(Gly332Ser)
CAMK2G NM_172169.2 -?/. - c.994G>A r.(?) p.(Gly332Ser)


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