Variant #0000885111 (NC_000002.11:g.27529106C>G, NM_002437.4:c.*3674G>C (MPV17))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.27529106C>G
DNA change (hg38) -
Published as TRIM54(NM_032546.3):c.1018C>G (p.(Leu340Val))
ISCN -
DB-ID MPV17_000027
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) 0.00019 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-11-01 13:01:21 +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.*3674G>C r.(=) p.(=)
UCN NM_003353.2 -?/. - c.*1283G>C r.(=) p.(=)
TRIM54 NM_187841.2 -?/. - c.892C>G r.(?) p.(Leu298Val)


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