Variant #0000979141 (NC_000010.10:g.75577316T>G, NC_000010.10(NM_172169.2):c.1181-4A>C (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.75577316T>G
DNA change (hg38) -
Published as CAMK2G(NM_001367534.1):c.1364-4A>C
ISCN -
DB-ID CAMK2G_000012
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) 0 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
CAMK2G NM_001367543.1 -?/. - c.1250-4A>C r.spl? p.?
CAMK2G NM_172169.2 -?/. - c.1181-4A>C r.spl? p.?


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