Variant #0000301215 (NC_000019.9:g.54407916_54407918del, NM_002739.3:c.1684_1686del (PRKCG))

Chromosome 19
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.54407916_54407918del
DNA change (hg38) g.53904662_53904664del
Published as PRKCG(NM_002739.3):c.1684_1686delGAG (p.E562del)
ISCN -
DB-ID PRKCG_000020
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRKCG NM_002739.3 ?/. - c.1684_1686del r.(?) p.(Glu562del)
CACNG7 NM_031896.4 ?/. - c.-8170_-8168del r.(?) p.(=)


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