Variant #0001033250 (NC_000002.11:g.27534800_27534812del, NM_002437.4:c.416_428del (MPV17))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.27534800_27534812del
DNA change (hg38) -
Published as MPV17(NM_002437.5):c.416_428del (p.(Pro139Glnfs*75))
ISCN -
DB-ID MPV17_000032
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 2025-05-05 21:14:00 +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     
MPV17 NM_002437.4 +?/. - c.416_428del r.(?) p.(Pro139Glnfs*75)
UCN NM_003353.2 +?/. - c.-3798_-3786del r.(?) p.(=)
TRIM54 NM_187841.2 +?/. - c.*5047_*5059del r.(=) p.(=)


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