Variant #0000335579 (NC_000023.10:g.132888056T>C, NM_004484.3:c.485A>G (GPC3))

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.132888056T>C
DNA change (hg38) g.133754029T>C
Published as GPC3(NM_001164617.1):c.485A>G (p.N162S), GPC3(NM_001164617.2):c.485A>G (p.N162S), GPC3(NM_004484.3):c.485A>G (p.(Asn162Ser))
ISCN -
DB-ID GPC3_000070 See all 3 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) 2.0E-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 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPC3 NM_004484.3 -?/. - c.485A>G r.(?) p.(Asn162Ser)


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