Variant #0000996805 (NC_000007.13:g.99687246dup, NM_004722.3:c.-12092dup (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.99687246dup
DNA change (hg38) -
Published as COPS6(NM_006833.4):c.211dupG (p.(Ala71fs))
ISCN -
DB-ID AP4M1_000069
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 2024-08-28 13:16:32 +02:00 (CEST)
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.-12092dup r.(?) p.(=)
MCM7 NM_005916.4 ?/. - c.*3312dup r.(?) p.(=)
COPS6 NM_006833.4 ?/. - c.211dup r.(?) p.(Ala71Glyfs*18)


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