Variant #0000654047 (NC_000001.10:g.45243414G>A, NM_153274.2:c.*6468C>T (BEST4))

Chromosome 1
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.45243414G>A
DNA change (hg38) g.44777742G>A
Published as RPS8(NM_001012.1):c.340G>A (p.(Glu114Lys))
ISCN -
DB-ID BEST4_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 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPS8 NM_001012.1 ?/. - c.340G>A r.(?) p.(Glu114Lys)
BEST4 NM_153274.2 ?/. - c.*6468C>T r.(=) p.(=)


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