Variant #0000890678 (NC_000012.11:g.53447242G>A, NC_000012.11(NM_170754.2):c.261+9G>A (TENC1))

Chromosome 12
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.53447242G>A
DNA change (hg38) -
Published as TNS2(NM_015319.2):c.291+9G>A
ISCN -
DB-ID EIF4B_000007
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) 0.00105 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +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     
EIF4B NM_001417.4 -?/. - c.*13235G>A r.(=) p.(=)
SPRYD3 NM_032840.2 -?/. - c.*12374C>T r.(=) p.(=)
TENC1 NM_170754.2 -?/. - c.261+9G>A r.(=) p.(=)


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