Variant #0000962062 (NC_000002.11:g.27535123A>C, NC_000002.11(NM_002437.4):c.376-9T>G (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.27535123A>C
DNA change (hg38) -
Published as MPV17(NM_002437.5):c.376-9T>G
ISCN -
DB-ID MPV17_000016 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) 1.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-02-26 20:06:56 +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.376-9T>G r.(=) p.(=)
UCN NM_003353.2 +?/. - c.-4109T>G r.(?) p.(=)
TRIM54 NM_187841.2 +?/. - c.*5370A>C r.(=) p.(=)


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