Variant #0000994497 (NC_000004.11:g.9218420G>C, NM_001256854.1:c.1290G>C (USP17L11))

Chromosome 4
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.9218420G>C
DNA change (hg38) -
Published as USP17L11(NM_001256854.1):c.1290G>C (p.(Gln430His))
ISCN -
DB-ID USP17L11_000018
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
USP17L10 NM_001256852.1 -?/. - c.*4445G>C r.(=) p.(=)
USP17L12 NM_001256853.1 -?/. - c.-3458G>C r.(?) p.(=)
USP17L11 NM_001256854.1 -?/. - c.1290G>C r.(?) p.(Gln430His)


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