Variant #0000851800 (NC_000008.10:g.133883593G>T, NM_003235.4:c.275G>T (TG))

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.133883593G>T
DNA change (hg38) -
Published as TG(NM_003235.4):c.275G>T (p.C92F), TG(NM_003235.5):c.275G>T (p.C92F)
ISCN -
DB-ID TG_000094 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) 1.0E-5 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 15:40:45 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLA NM_001045556.2 ?/. - c.*167176C>A r.(=) p.(=)
TG NM_003235.4 ?/. - c.275G>T r.(?) p.(Cys92Phe)


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