Variant #0000888069 (NC_000007.13:g.99705159C>T, NM_004722.3:c.*654C>T (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.99705159C>T
DNA change (hg38) -
Published as AP4M1(NM_004722.4):c.*654C>T
ISCN -
DB-ID AP4M1_000067
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:01:21 +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.*654C>T r.(=) p.(=)
TAF6 NM_005641.3 ?/. - c.1744G>A r.(?) p.(Val582Ile)
MCM7 NM_005916.4 ?/. - c.-6242G>A r.(?) p.(=)
CNPY4 NM_152755.1 ?/. - c.-12209C>T r.(?) p.(=)


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