Variant #0000523537 (NC_000004.11:g.9217197T>C, NM_001256854.1:c.67T>C (USP17L11))

Chromosome 4
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.9217197T>C
DNA change (hg38) g.9215471T>C
Published as USP17L11(NM_001256854.1):c.67T>C (p.S23P)
ISCN -
DB-ID USP17L11_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) 0.05042 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
USP17L10 NM_001256852.1 -/. - c.*3222T>C r.(=) p.(=)
USP17L12 NM_001256853.1 -/. - c.-4681T>C r.(?) p.(=)
USP17L11 NM_001256854.1 -/. - c.67T>C r.(?) p.(Ser23Pro)


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