Variant #0000291396 (NC_000023.10:g.77150939_77150940del, NM_032121.5:c.65_66del (MAGT1))

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.77150939_77150940del
DNA change (hg38) g.77895442_77895443del
Published as MAGT1(NM_032121.5):c.65_66delAA (p.K22Sfs*49)
ISCN -
DB-ID MAGT1_000010
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-20 15:46:09 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COX7B NM_001866.2 ?/. - c.-4112_-4111del r.(?) p.(=)
MAGT1 NM_032121.5 ?/. - c.65_66del r.(?) p.(Lys22SerfsTer49)


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