Variant #0000535296 (NC_000008.10:g.7195434G>T, NM_001256873.1:c.*3933G>T (USP17L1P))

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.7195434G>T
DNA change (hg38) g.7337912G>T
Published as USP17L4(NM_001256874.1):c.798G>T (p.T266=)
ISCN -
DB-ID USP17L1P_000005
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) 0.0005 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     
USP17L1P NM_001256873.1 -?/. - c.*3933G>T r.(=) p.(=)
USP17L4 NM_001256874.1 -?/. - c.798G>T r.(?) p.(Thr266=)
FAM66B NR_027423.1 -?/. - n.608+11171C>A r.(?) -


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