Variant #0000619010 (NC_000023.10:g.132440086_132440087insAT, NM_001448.2:c.974_975insTA (GPC4))

Chromosome X
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.132440086_132440087insAT
DNA change (hg38) g.133306058_133306059insAT
Published as GPC4(NM_001448.2):c.974_975insTA (p.M326Tfs*69)
ISCN -
DB-ID GPC4_000017
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-21 09:54:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPC4 NM_001448.2 ?/. - c.974_975insTA r.(?) p.(Met326ThrfsTer69)


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