Variant #0000982659 (NC_000017.10:g.57288347T>C, NM_018149.6:c.935T>C (SMG8))

Chromosome 17
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.57288347T>C
DNA change (hg38) -
Published as SMG8(NM_018149.7):c.935T>C (p.(Phe312Ser))
ISCN -
DB-ID PRR11_000006
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMG8 NM_018149.6 ?/. - c.935T>C r.(?) p.(Phe312Ser)
PRR11 NM_018304.3 ?/. - c.*9355T>C r.(=) p.(=)


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