Variant #0000325365 (NC_000017.10:g.36887055C>G, NM_007144.2:c.*4421G>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.36887055C>G
DNA change (hg38) g.38730802C>G
Published as CISD3(NM_001136498.1):c.84+7C>G (p.(=))
ISCN -
DB-ID CISD3_000001
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) 7.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CISD3 NM_001136498.1 ?/. - c.84+7C>G r.(=) p.(=)
MLLT6 NM_005937.3 ?/. - c.*5204C>G r.(=) p.(=)
PCGF2 NM_007144.2 ?/. - c.*4421G>C r.(=) p.(=)


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