Variant #0001050558 (NC_000002.11:g.27535926G>A, NM_002437.4:c.121C>T (MPV17))

Chromosome 2
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.27535926G>A
DNA change (hg38) -
Published as MPV17(NM_002437.5):c.121C>T (p.(Arg41Trp))
ISCN -
DB-ID MPV17_000035
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MPV17 NM_002437.4 +/. - c.121C>T r.(?) p.(Arg41Trp)
UCN NM_003353.2 +/. - c.-4912C>T r.(?) p.(=)
TRIM54 NM_187841.2 +/. - c.*6173G>A r.(=) p.(=)


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