Variant #0000856772 (NC_000023.10:g.70836515G>T, NM_052957.4:c.*3683G>T (ACRC))

Chromosome X
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.70836515G>T
DNA change (hg38) -
Published as CXCR3(NM_001142797.1):c.948C>A (p.T316=)
ISCN -
DB-ID ACRC_000041
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) 7.0E-5 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 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CXCR3 NM_001142797.1 -?/. - c.948C>A r.(?) p.(Thr316=)
ACRC NM_052957.4 -?/. - c.*3683G>T r.(=) p.(=)


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