Variant #0001038663 (NC_000011.9:g.67168308C>T, NM_002708.3:c.270G>A (PPP1CA))

Chromosome 11
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.67168308C>T
DNA change (hg38) -
Published as PPP1CA(NM_002708.4):c.270G>A (p.(Leu90=))
ISCN -
DB-ID PPP1CA_000005
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) 0.00347 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 2025-05-05 21:14:00 +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     
PPP1CA NM_002708.3 -?/. - c.270G>A r.(?) p.(=)
RAD9A NM_004584.2 -?/. - c.*3278C>T r.(=) p.(=)
TBC1D10C NM_198517.3 -?/. - c.-3133C>T r.(?) p.(=)


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