Variant #0000335925 (NC_000023.10:g.151303743G>T, NM_021049.4:c.-17504C>A (MAGEA5))

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.151303743G>T
DNA change (hg38) g.152135271G>T
Published as MAGEA10(NM_001011543.2):c.350C>A (p.(Pro117Gln))
ISCN -
DB-ID MAGEA10_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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
MAGEA10 NM_021048.4 -?/. - c.350C>A r.(?) p.(Pro117Gln)
MAGEA5 NM_021049.4 -?/. - c.-17504C>A r.(?) p.(=)


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