Variant #0000718726 (NC_000002.11:g.27535925C>T, NM_002437.4:c.122G>A (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.27535925C>T
DNA change (hg38) -
Published as MPV17(NM_002437.5):c.122G>A (p.R41Q)
ISCN -
DB-ID MPV17_000015 See all 9 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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MPV17 NM_002437.4 +/. - c.122G>A r.(?) p.(Arg41Gln)
UCN NM_003353.2 +/. - c.-4911G>A r.(?) p.(=)
TRIM54 NM_187841.2 +/. - c.*6172C>T r.(=) p.(=)


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