Variant #0000979794 (NC_000011.9:g.67809268C>T, NM_006019.3:c.166C>T (TCIRG1))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.67809268C>T
DNA change (hg38) -
Published as TCIRG1(NM_006019.2):c.166C>T (p.R56W), TCIRG1(NM_006019.3):c.166C>T (p.(Arg56Trp)), TCIRG1(NM_006019.4):c.166C>T (p.R56W)
ISCN -
DB-ID TCIRG1_000015 See all 5 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) 0.04644 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TCIRG1 NM_006019.3 -/. - c.166C>T r.(?) p.(Arg56Trp)


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