Variant #0000331725 (NC_000007.13:g.99696224G>A, NM_004722.3:c.-3114G>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.99696224G>A
DNA change (hg38) g.100098601G>A
Published as MCM7(NM_001278595.1):c.169C>T (p.(Gln57Ter))
ISCN -
DB-ID MCM7_000001
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.-3114G>A r.(?) p.(=)
TAF6 NM_005641.3 ?/. - c.*8645C>T r.(=) p.(=)
MCM7 NM_005916.3 ?/. - c.697C>T r.(?) p.(Gln233Ter)
MCM7 NM_005916.4 ?/. - c.697C>T r.(?) p.(Gln233Ter)


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