Variant #0000574088 (NC_000023.10:g.149013272G>A, NM_001166400.1:c.226G>A (MAGEA8))

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.149013272G>A
DNA change (hg38) g.149884498G>A
Published as MAGEA8(NM_001166400.1):c.226G>A (p.D76N)
ISCN -
DB-ID MAGEA8-AS1_000002
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAGEA8 NM_001166400.1 -?/. - c.226G>A r.(?) p.(Asp76Asn)
MAGEA8-AS1 NR_102703.1 -?/. - n.81-2000C>T r.(?) -


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