Variant #0000679808 (NC_000013.10:g.37581147C>T, NM_181503.2:c.426C>T (EXOSC8))

Chromosome 13
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.37581147C>T
DNA change (hg38) -
Published as EXOSC8(NM_181503.3):c.426C>T (p.L142=)
ISCN -
DB-ID EXOSC8_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) 0.00219 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SUPT20H NM_017569.3 -?/. - c.*2699G>A r.(=) p.(=)
EXOSC8 NM_181503.2 -?/. - c.426C>T r.(?) p.(Leu142=)


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