Variant #0000333565 (NC_000023.10:g.30261241T>C, NM_002363.4:c.-927T>C (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.30261241T>C
DNA change (hg38) g.30243124T>C
Published as MAGEB4(NM_002367.3):c.989T>C (p.(Met330Thr))
ISCN -
DB-ID MAGEB4_000008
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) 0.0021 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     
MAGEB1 NM_002363.4 -?/. - c.-927T>C r.(?) p.(=)
MAGEB4 NM_002367.3 -?/. - c.989T>C r.(?) p.(Met330Thr)


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