Variant #0000535351 (NC_000008.10:g.7829539G>A, NM_001256872.1:c.1237C>T (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.7829539G>A
DNA change (hg38) g.7972017G>A
Published as USP17L8(NM_001256872.1):c.1237C>T (p.P413S)
ISCN -
DB-ID USP17L8_000004
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) 0.43232 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.*4376C>T r.(=) p.(=)
USP17L8 NM_001256872.1 -/. - c.1237C>T r.(?) p.(Pro413Ser)
FAM66E NR_027424.1 -/. - n.610+10721G>A r.(?) -


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