Variant #0000439017 (NC_000001.10:g.27120790C>T, NM_017837.3:c.265C>T (PIGV))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.27120790C>T
DNA change (hg38) g.26794299C>T
Published as -
ISCN -
DB-ID PIGV_000025 See all 2 reported entries
Variant remarks -
Reference PubMed: Knaus et al. 2018
ClinVar ID -
dbSNP ID -
Origin Germline/De novo (untested)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Philippe Campeau
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Philippe Campeau
Date created 2018-12-03 22:29:15 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIGV NM_017837.3 +?/+? - c.265C>T r.(?) p.(Pro89Ser)


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