Variant #0000291737 (NC_000007.13:g.100028971G>A, NM_017984.4:c.-2917C>T (ZCWPW1))

Chromosome 7
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.100028971G>A
DNA change (hg38) g.100431348G>A
Published as MEPCE(NM_019606.6):c.1330G>A (p.G444S)
ISCN -
DB-ID MEPCE_000003
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZCWPW1 NM_017984.4 ?/. - c.-2917C>T r.(?) p.(=)
MEPCE NM_019606.5 ?/. - c.1330G>A r.(?) p.(Gly444Ser)
PPP1R35 NM_145030.2 ?/. - c.*4012C>T r.(=) p.(=)


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