Variant #0000306395 (NC_000019.9:g.54410134T>C, NM_002739.3:c.2079T>C (PRKCG))

Chromosome 19
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.54410134T>C
DNA change (hg38) g.53906880T>C
Published as PRKCG(NM_002739.3):c.2079T>C (p.P693=)
ISCN -
DB-ID PRKCG_000025
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-16 13:23:31 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRKCG NM_002739.3 -?/. - c.2079T>C r.(?) p.(Pro693=)
CACNG7 NM_031896.4 -?/. - c.-5952T>C r.(?) p.(=)


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