Variant #0000619079 (NC_000023.10:g.140994171_140994172del, NM_005462.4:c.981_982del (MAGEC1))

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.140994171_140994172del
DNA change (hg38) g.141906385_141906386del
Published as MAGEC1(NM_005462.4):c.979_980del (p.(His327GlnfsTer4))
ISCN -
DB-ID MAGEC1_000101
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-21 10:37:10 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAGEC1 NM_005462.4 ?/. - c.981_982del r.(?) p.(His327GlnfsTer4)


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