Variant #0000894064 (NC_000017.10:g.57287667T>C, NM_018149.6:c.255T>C (SMG8))

Chromosome 17
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.57287667T>C
DNA change (hg38) -
Published as SMG8(NM_018149.7):c.255T>C (p.P85=)
ISCN -
DB-ID PRR11_000002
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) 0.00173 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMG8 NM_018149.6 -?/. - c.255T>C r.(?) p.(Pro85=)
PRR11 NM_018304.3 -?/. - c.*8675T>C r.(=) p.(=)


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