Variant #0000690321 (NC_000008.10:g.7195171G>A, NM_001256873.1:c.*3670G>A (USP17L1P))

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.7195171G>A
DNA change (hg38) -
Published as USP17L4(NM_001256874.1):c.535G>A (p.G179S)
ISCN -
DB-ID USP17L1P_000009
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) 0.00013 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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
USP17L1P NM_001256873.1 ?/. - c.*3670G>A r.(=) p.(=)
USP17L4 NM_001256874.1 ?/. - c.535G>A r.(?) p.(Gly179Ser)
FAM66B NR_027423.1 ?/. - n.608+11434C>T r.(?) -


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