Variant #0001042201 (NC_000017.10:g.7487199G>T, NM_004870.3:c.19G>T (MPDU1))

Chromosome 17
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.7487199G>T
DNA change (hg38) -
Published as MPDU1(NM_004870.4):c.19G>T (p.(Gly7*))
ISCN -
DB-ID MPDU1_000019
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 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     
CD68 NM_001251.2 ?/. - c.*2370G>T r.(=) p.(=)
EIF4A1 NM_001416.3 ?/. - c.*5395G>T r.(=) p.(=)
MPDU1 NM_004870.3 ?/. - c.19G>T r.(?) p.(Gly7*)
SOX15 NM_006942.1 ?/. - c.*4497C>A r.(=) p.(=)
SENP3 NM_015670.5 ?/. - c.*12398G>T r.(=) p.(=)


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