Variant #0000679992 (NC_000014.8:g.57706331del, NM_018229.3:c.-29702del (AP5M1))

Chromosome 14
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.57706331del
DNA change (hg38) -
Published as EXOC5(NM_006544.3):c.513del (p.(Glu172Serfs*21))
ISCN -
DB-ID AP5M1_000002
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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EXOC5 NM_006544.3 ?/. - c.513del r.(?) p.(Glu172SerfsTer21)
AP5M1 NM_018229.3 ?/. - c.-29702del r.(?) p.(=)


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