Variant #0000342671 (NC_000007.13:g.99703901C>T, NM_004722.3:c.1012C>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.99703901C>T
DNA change (hg38) g.100106278C>T
Published as AP4M1(NM_004722.3):c.1012C>T (p.R338*), AP4M1(NM_004722.4):c.1012C>T (p.(Arg338*))
ISCN -
DB-ID AP4M1_000003 See all 5 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) 4.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AP4M1 NM_004722.3 +/. - c.1012C>T r.(?) p.(Arg338Ter)
TAF6 NM_005641.3 +/. - c.*968G>A r.(=) p.(=)
MCM7 NM_005916.3 +/. - c.-4984G>A r.(?) p.(=)
MCM7 NM_005916.4 +/. - c.-4984G>A r.(?) p.(=)
CNPY4 NM_152755.1 +/. - c.-13467C>T r.(?) p.(=)


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