Variant #0000852572 (NC_000010.10:g.75612995T>C, NM_172169.2:c.230A>G (CAMK2G))

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.75612995T>C
DNA change (hg38) -
Published as CAMK2G(NM_172171.3):c.230A>G (p.H77R)
ISCN -
DB-ID CAMK2G_000006
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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CAMK2G NM_001367543.1 ?/. - c.230A>G r.(?) p.(His77Arg)
CAMK2G NM_172169.2 ?/. - c.230A>G r.(?) p.(His77Arg)


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