Variant #0000854577 (NC_000016.9:g.624108G>A, NM_004204.3:c.34G>A (PIGQ))

Chromosome 16
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.624108G>A
DNA change (hg38) -
Published as PIGQ(NM_004204.3):c.34G>A (p.V12I)
ISCN -
DB-ID NHLRC4_000002
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) 0.00078 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +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     
PIGQ NM_004204.3 -?/. - c.34G>A r.(?) p.(Val12Ile)
NHLRC4 NM_176677.1 -?/. - c.*5689G>A r.(=) p.(=)


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