Variant #0000577334 (NC_000023.10:g.70837023G>A, NM_052957.4:c.*4191G>A (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.70837023G>A
DNA change (hg38) g.71617173G>A
Published as CXCR3(NM_001142797.1):c.440C>T (p.T147M, p.(Thr147Met))
ISCN -
DB-ID CXCR3_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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CXCR3 NM_001142797.1 -?/. - c.440C>T r.(?) p.(Thr147Met)
ACRC NM_052957.4 -?/. - c.*4191G>A r.(=) p.(=)


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