Variant #0000803328 (NC_000007.13:g.99697682C>A, NM_004722.3:c.-1656C>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.99697682C>A
DNA change (hg38) -
Published as MCM7(NM_005916.4):c.66G>T (p.Q22H)
ISCN -
DB-ID AP4M1_000060
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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AP4M1 NM_004722.3 ?/. - c.-1656C>A r.(?) p.(=)
TAF6 NM_005641.3 ?/. - c.*7187G>T r.(=) p.(=)
MCM7 NM_005916.3 ?/. - c.66G>T r.(?) p.(Gln22His)
MCM7 NM_005916.4 ?/. - c.66G>T r.(?) p.(Gln22His)


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