Variant #0000856770 (NC_000023.10:g.70800708G>A, NM_052957.4:c.37G>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.70800708G>A
DNA change (hg38) -
Published as GCNA(NM_052957.4):c.37G>A (p.E13K)
ISCN -
DB-ID OGT_000024
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) 1.0E-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     
ACRC NM_052957.4 -?/. - c.37G>A r.(?) p.(Glu13Lys)
OGT NM_181672.2 -?/. - c.*7064G>A r.(=) p.(=)


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