Variant #0000515542 (NC_000002.11:g.27535883A>G, NM_002437.4:c.164T>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.27535883A>G
DNA change (hg38) g.27313016A>G
Published as MPV17(NM_002437.4):c.164T>C (p.(Val55Ala))
ISCN -
DB-ID MPV17_000018
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) 8.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +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.164T>C r.(?) p.(Val55Ala)
UCN NM_003353.2 -?/. - c.-4869T>C r.(?) p.(=)
TRIM54 NM_187841.2 -?/. - c.*6130A>G r.(=) p.(=)


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