Variant #0000534172 (NC_000008.10:g.145139325G>C, NM_003801.3:c.823G>C (GPAA1))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.145139325G>C
DNA change (hg38) g.144084422G>C
Published as GPAA1(NM_003801.3):c.823G>C (p.(Glu275Gln))
ISCN -
DB-ID EXOSC4_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) 0.00901 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPAA1 NM_003801.3 -?/. - c.823G>C r.(?) p.(Glu275Gln)
EXOSC4 NM_019037.2 -?/. - c.*3821G>C r.(=) p.(=)


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