Variant #0000726319 (NC_000017.10:g.36894658A>G, NM_007144.2:c.524T>C (PCGF2))

Chromosome 17
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.36894658A>G
DNA change (hg38) -
Published as PCGF2(NM_007144.3):c.524T>C (p.M175T)
ISCN -
DB-ID CISD3_000002
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CISD3 NM_001136498.1 ?/. - c.*4950A>G r.(=) p.(=)
PCGF2 NM_007144.2 ?/. - c.524T>C r.(?) p.(Met175Thr)


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