Variant #0000719923 (NC_000004.11:g.527659_527660del, NM_001127178.1:c.2624_2625del (PIGG))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.527659_527660del
DNA change (hg38) -
Published as PIGG(NM_001127178.3):c.2624_2625delTA (p.L875*), PIGG(NM_001345994.2):c.1526_1527delTA (p.L509*)
ISCN -
DB-ID PIGG_000022 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) 0.0001 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.2624_2625del r.(?) p.(Leu875Ter)


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