Variant #0000656889 (NC_000011.9:g.67817647T>A, NM_006019.3:c.2162T>A (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.67817647T>A
DNA change (hg38) g.68050180T>A
Published as TCIRG1(NM_006019.2):c.2162T>A (p.I721N), TCIRG1(NM_006019.3):c.2162T>A (p.(Ile721Asn))
ISCN -
DB-ID CHKA_000002 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHKA NM_001277.2 ?/. - c.*3808A>T r.(=) p.(=)
TCIRG1 NM_006019.3 ?/. - c.2162T>A r.(?) p.(Ile721Asn)


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