Variant #0000810642 (NC_000023.10:g.70832329G>A, NM_052957.4:c.1875G>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.70832329G>A
DNA change (hg38) -
Published as GCNA(NM_052957.4):c.1875G>A (p.P625=)
ISCN -
DB-ID ACRC_000035
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) 0.00013 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 2021-09-17 14:40:49 +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.*3886C>T r.(=) p.(=)
ACRC NM_052957.4 -?/. - c.1875G>A r.(?) p.(Pro625=)


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