Variant #0000619451 (NC_000023.10:g.30260504C>T, NM_002363.4:c.-1664C>T (MAGEB1))

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.30260504C>T
DNA change (hg38) g.30242387C>T
Published as MAGEB4(NM_002367.3):c.252C>T (p.D84=)
ISCN -
DB-ID MAGEB3_000024
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) 8.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-17 21:30:54 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAGEB1 NM_002363.4 -?/. - c.-1664C>T r.(?) p.(=)
MAGEB3 NM_002365.4 -?/. - c.*5422C>T r.(=) p.(=)
MAGEB4 NM_002367.3 -?/. - c.252C>T r.(?) p.(Asp84=)


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