Variant #0000534174 (NC_000008.10:g.145140501_145140502del, NM_003801.3:c.1477_1478del (GPAA1))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.145140501_145140502del
DNA change (hg38) g.144085598_144085599del
Published as -
ISCN -
DB-ID EXOSC4_000003
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) 0.00013 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-24 19:00:13 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPAA1 NM_003801.3 +?/. - c.1477_1478del r.(?) p.(Arg493GlyfsTer152)
EXOSC4 NM_019037.2 +?/. - c.*4997_*4998del r.(=) p.(=)


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