Variant #0000867050 (NC_000023.10:g.132445391G>A, NM_001448.2:c.772C>T (GPC4))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.132445391G>A
DNA change (hg38) -
Published as GPC4(NM_001448.2):c.772C>T (p.(Arg258Trp)), GPC4(NM_001448.3):c.772C>T (p.R258W)
ISCN -
DB-ID GPC4_000012 See all 2 reported entries
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) 0.00044 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPC4 NM_001448.2 -?/. - c.772C>T r.(?) p.(Arg258Trp)


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