Variant #0000619135 (NC_000023.10:g.151304077T>C, NM_021049.4:c.-17838A>G (MAGEA5))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.151304077T>C
DNA change (hg38) g.152135605T>C
Published as MAGEA10(NM_001011543.2):c.16A>G (p.K6E)
ISCN -
DB-ID MAGEA5_000014
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) 2.0E-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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAGEA10 NM_021048.4 ?/. - c.16A>G r.(?) p.(Lys6Glu)
MAGEA5 NM_021049.4 ?/. - c.-17838A>G r.(?) p.(=)


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