Variant #0000282577 (NC_000002.11:g.27535313dup, NC_000002.11(NM_002437.4):c.375+49dup (MPV17))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.27535313dup
DNA change (hg38) g.27312446dup
Published as MPV17(NM_002437.5):c.375+49dupC
ISCN -
DB-ID MPV17_000013
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MPV17 NM_002437.4 -/. - c.375+49dup r.(=) p.(=)
UCN NM_003353.2 -/. - c.-4298dup r.(?) p.(=)
TRIM54 NM_187841.2 -/. - c.*5560dup r.(?) p.(=)


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