Variant #0000723663 (NC_000011.9:g.67817678C>T, NM_006019.3:c.2193C>T (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.67817678C>T
DNA change (hg38) -
Published as TCIRG1(NM_001351059.1):c.1299C>T (p.T433=), TCIRG1(NM_006019.2):c.2193C>T (p.T731=)
ISCN -
DB-ID CHKA_000011 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) 0.00066 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHKA NM_001277.2 -?/. - c.*3777G>A r.(=) p.(=)
TCIRG1 NM_006019.3 -?/. - c.2193C>T r.(?) p.(Thr731=)


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