Variant #0000538091 (NC_000009.11:g.35095372G>A, NM_032634.3:c.191C>T (PIGO))

Chromosome 9
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.35095372G>A
DNA change (hg38) g.35095375G>A
Published as PIGO(NM_001201484.1):c.191C>T (p.(Ala64Val))
ISCN -
DB-ID PIGO_000039
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STOML2 NM_013442.1 -?/. - c.*4660C>T r.(=) p.(=)
PIGO NM_032634.3 -?/. - c.191C>T r.(?) p.(Ala64Val)


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