Variant #0000890124 (NC_000011.9:g.67815178_67815192del, NM_006019.3:c.1370_1384del (TCIRG1))

Chromosome 11
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.67815178_67815192del
DNA change (hg38) -
Published as TCIRG1(NM_006019.3):c.1362_1376del (p.(Thr457_Tyr461del))
ISCN -
DB-ID TCIRG1_000051
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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TCIRG1 NM_006019.3 ?/. - c.1370_1384del r.(?) p.(Thr457_Tyr461del)


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