Variant #0001052751 (NC_000007.13:g.99700579T>C, NM_004722.3:c.347T>C (AP4M1))

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.99700579T>C
DNA change (hg38) -
Published as AP4M1(NM_004722.4):c.347T>C (p.(Val116Ala))
ISCN -
DB-ID AP4M1_000074
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) 1.0E-5 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 2025-11-01 13:22:20 +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.347T>C r.(?) p.(Val116Ala)
TAF6 NM_005641.3 ?/. - c.*4290A>G r.(=) p.(=)
MCM7 NM_005916.4 ?/. - c.-1662A>G r.(?) p.(=)
CNPY4 NM_152755.1 ?/. - c.-16789T>C r.(?) p.(=)


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