Variant #0000577512 (NC_000023.10:g.76939115G>C, ATRX(NM_000489.3):c.1633C>G)

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.76939115G>C
DNA change (hg38) g.77683623G>C
Published as ATRX(NM_000489.3):c.1633C>G (p.(Gln545Glu)), ATRX(NM_000489.5):c.1633C>G (p.Q545E)
ISCN -
DB-ID ATRX_000200 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) 0.00159 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATRX NM_000489.3 -?/. - c.1633C>G r.(?) p.(Gln545Glu)