Variant #0000545422 (NC_000011.9:g.67810474G>A, NM_006019.3:c.479G>A (TCIRG1))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.67810474G>A
DNA change (hg38) g.68043007G>A
Published as TCIRG1(NM_006019.3):c.479G>A (p.(Gly160Glu)), TCIRG1(NM_006019.4):c.479G>A (p.G160E)
ISCN -
DB-ID TCIRG1_000016 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) 0.00494 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +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.479G>A r.(?) p.(Gly160Glu)


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