Variant #0000340455 (NC_000023.10:g.76953085C>T, NM_000489.3:c.228G>A (ATRX))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.76953085C>T
DNA change (hg38) g.77697597C>T
Published as ATRX(NM_000489.3):c.228G>A (p.(Ser76=)), ATRX(NM_000489.6):c.228G>A (p.S76=)
ISCN -
DB-ID ATRX_000207 See all 3 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) 0.00759 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATRX NM_000489.3 -/. - c.228G>A r.(?) p.(Ser76=)


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