Variant #0000805346 (NC_000011.9:g.67818023C>T, NM_006019.3:c.2306C>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.67818023C>T
DNA change (hg38) -
Published as TCIRG1(NM_001351059.1):c.1412C>T (p.A471V), TCIRG1(NM_006019.3):c.2306C>T (p.(Ala769Val))
ISCN -
DB-ID CHKA_000012 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) 0.00037 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHKA NM_001277.2 -?/. - c.*3432G>A r.(=) p.(=)
TCIRG1 NM_006019.3 -?/. - c.2306C>T r.(?) p.(Ala769Val)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.