Variant #0000809358 (NC_000021.8:g.33671285G>A, NM_178817.3:c.3G>A (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.33671285G>A
DNA change (hg38) -
Published as MRAP(NM_178817.3):c.3G>A (p.M1?)
ISCN -
DB-ID MRAP_000009 See all 2 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) 6.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
URB1 NM_014825.2 +/. - c.*15944C>T r.(=) p.(=)
MRAP NM_178817.3 +/. - c.3G>A r.(?) p.(Met1?)


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