Variant #0000342743 (NC_000007.13:g.99704100G>A, NM_004722.3:c.1100G>A (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.99704100G>A
DNA change (hg38) g.100106477G>A
Published as -
ISCN -
DB-ID AP4M1_000038
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) 0.00034 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 2022-11-01 13:01:21 +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.1100G>A r.(?) p.(Arg367Gln)
TAF6 NM_005641.3 ?/. - c.*769C>T r.(=) p.(=)
MCM7 NM_005916.3 ?/. - c.-5183C>T r.(?) p.(=)
MCM7 NM_005916.4 ?/. - c.-5183C>T r.(?) p.(=)
CNPY4 NM_152755.1 ?/. - c.-13268G>A r.(?) p.(=)


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