Variant #0001025462 (NC_000007.13:g.99703582G>A, NM_004722.3:c.930G>A (AP4M1))

Chromosome 7
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.99703582G>A
DNA change (hg38) -
Published as AP4M1(NM_004722.3):c.930G>A (p.R310=), AP4M1(NM_004722.4):c.930G>A (p.R310=)
ISCN -
DB-ID AP4M1_000018 See all 2 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) 0.00073 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2025-02-07 18:57:27 +01:00 (CET)
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.930G>A r.(?) p.(Arg310=)
TAF6 NM_005641.3 -?/. - c.*1287C>T r.(=) p.(=)
MCM7 NM_005916.3 -?/. - c.-4665C>T r.(?) p.(=)
MCM7 NM_005916.4 -?/. - c.-4665C>T r.(?) p.(=)
CNPY4 NM_152755.1 -?/. - c.-13786G>A r.(?) p.(=)


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