Variant #0000308667 (NC_000005.9:g.176056806C>T, NM_001099408.1:c.-1461C>T (EIF4E1B))

Chromosome 5
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.176056806C>T
DNA change (hg38) g.176629805C>T
Published as SNCB(NM_001001502.2):c.-10+4G>A, SNCB(NM_001001502.3):c.-10+4G>A
ISCN -
DB-ID SNCB_000002 See all 2 reported entries
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +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     
SNCB NM_001001502.1 -/. - c.-10+4G>A r.spl? p.?
EIF4E1B NM_001099408.1 -/. - c.-1461C>T r.(?) p.(=)


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