Variant #0000291968 (NC_000021.8:g.33671389del, NC_000021.8(NM_178817.3):c.106+1del (MRAP))

Chromosome 21
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.33671389del
DNA change (hg38) g.32299078del
Published as MRAP(NM_178817.3):c.106+1delG
ISCN -
DB-ID MRAP_000001 See all 3 reported entries
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 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-16 22:01:57 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
URB1 NM_014825.2 +/. - c.*15840del r.(?) p.(=)
MRAP NM_178817.3 +/. - c.106+1del r.spl? p.?


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