Variant #0000311113 (NC_000017.10:g.26875677G>C, NM_005148.3:c.267C>G (UNC119))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.26875677G>C
DNA change (hg38) g.28548659G>C
Published as UNC119(NM_054035.2):c.267C>G (p.V89=)
ISCN -
DB-ID UNC119_000004 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) 0.00097 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-13 11:10:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UNC119 NM_005148.3 -/. - c.267C>G r.(?) p.(Val89=)
PIGS NM_033198.3 -/. - c.*5561C>G r.(=) p.(=)


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