Variant #0000522641 (NC_000004.11:g.494339_494340del, NM_001127178.1:c.309_310del (PIGG))

Chromosome 4
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.494339_494340del
DNA change (hg38) g.500550_500551del
Published as PIGG(NM_001127178.1):c.307_308del (p.(His103GlnfsTer5))
ISCN -
DB-ID PIGG_000008
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIGG NM_001127178.1 ?/. - c.309_310del r.(?) p.(His103GlnfsTer5)
ZNF721 NM_133474.2 ?/. - c.-1587_-1586del r.(?) p.(=)


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