Variant #0000535349 (NC_000008.10:g.7829388A>G, NM_001256872.1:c.1388T>C (USP17L8))

Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.7829388A>G
DNA change (hg38) g.7971866A>G
Published as USP17L8(NM_001256872.1):c.1388T>C (p.V463A)
ISCN -
DB-ID USP17L8_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) 0.2942 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
USP17L3 NM_001256871.1 -/. - c.*4527T>C r.(=) p.(=)
USP17L8 NM_001256872.1 -/. - c.1388T>C r.(?) p.(Val463Ala)
FAM66E NR_027424.1 -/. - n.610+10570A>G r.(?) -


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