Variant #0001035983 (NC_000007.13:g.100205261G>A, NM_023948.4:c.-5154G>A (MOSPD3))

Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.100205261G>A
DNA change (hg38) -
Published as PCOLCE(NM_002593.4):c.1014G>A (p.(Val338=))
ISCN -
DB-ID MOSPD3_000001
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) 0.0046 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCOLCE NM_002593.3 ?/. - c.1014G>A r.(?) p.(=)
MOSPD3 NM_023948.4 ?/. - c.-5154G>A r.(?) p.(=)


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