Variant #0000690166 (NC_000008.10:g.133882008del, NM_003235.4:c.211del (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.133882008del
DNA change (hg38) -
Published as TG(NM_003235.4):c.211delT (p.W71Gfs*35)
ISCN -
DB-ID TG_000158
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 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 2020-09-15 15:50:26 +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.*168761del r.(?) p.(=)
TG NM_003235.4 +?/. - c.211del r.(?) p.(Trp71GlyfsTer35)


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