Variant #0000561483 (NC_000017.10:g.40489548_40489549del, STAT3(NM_139276.2):c.704_705del)

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.40489548_40489549del
DNA change (hg38) g.42337530_42337531del
Published as STAT3(NM_139276.2):c.704_705delTC (p.L235Hfs*7)
ISCN -
DB-ID STAT3_000057
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STAT3 NM_139276.2 +/. - c.704_705del r.(?) p.(Leu235HisfsTer7)