Variant #0000978279 (NC_000008.10:g.7215520C>G, NM_001256873.1:c.*24019C>G (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.7215520C>G
DNA change (hg38) -
Published as ZNF705G(NM_001164457.3):c.881G>C (p.(Ser294Thr))
ISCN -
DB-ID USP17L1P_000010
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) 0.0008 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
ZNF705G NM_001164457.1 -?/. - c.881G>C r.(?) p.(Ser294Thr)
USP17L1P NM_001256873.1 -?/. - c.*24019C>G r.(=) p.(=)
USP17L4 NM_001256874.1 -?/. - c.*19291C>G r.(=) p.(=)


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