Variant #0000315437 (NC_000023.10:g.52895603_52895606del, NC_000023.10(NM_133179.2):c.82-16_82-13del (XAGE3))

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.52895603_52895606del
DNA change (hg38) g.52866574_52866577del
Published as XAGE3(NM_133179.3):c.82-16_82-13delACAC
ISCN -
DB-ID XAGE3_000034
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
XAGE3 NM_133179.2 -?/. - c.82-16_82-13del r.(=) p.(=)


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