Variant #0000996809 (NC_000007.13:g.99703604C>T, NM_004722.3:c.952C>T (AP4M1))

Chromosome 7
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.99703604C>T
DNA change (hg38) -
Published as AP4M1(NM_004722.3):c.952C>T (p.(Arg318*)), AP4M1(NM_004722.4):c.952C>T (p.R318*)
ISCN -
DB-ID AP4M1_000004 See all 6 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) 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 2024-08-28 13:16:32 +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     
AP4M1 NM_004722.3 +/. - c.952C>T r.(?) p.(Arg318Ter)
TAF6 NM_005641.3 +/. - c.*1265G>A r.(=) p.(=)
MCM7 NM_005916.3 +/. - c.-4687G>A r.(?) p.(=)
MCM7 NM_005916.4 +/. - c.-4687G>A r.(?) p.(=)
CNPY4 NM_152755.1 +/. - c.-13764C>T r.(?) p.(=)


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