Variant #0000996940 (NC_000008.10:g.133899528G>T, NM_003235.4:c.1911G>T (TG))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.133899528G>T
DNA change (hg38) -
Published as TG(NM_003235.4):c.1911G>T (p.(Trp637Cys)), TG(NM_003235.5):c.1911G>T (p.W637C)
ISCN -
DB-ID TG_000102 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) 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 2024-08-28 13:16:32 +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     
SLA NM_001045556.2 +?/. - c.*151241C>A r.(=) p.(=)
TG NM_003235.4 +?/. - c.1911G>T r.(?) p.(Trp637Cys)


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