Variant #0000976200 (NC_000004.11:g.166978397G>A, NM_001204760.1:c.*26772G>A (TLL1))

Chromosome 4
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.166978397G>A
DNA change (hg38) -
Published as TLL1(NM_012464.4):c.1782G>A (p.L594=), TLL1(NM_012464.5):c.1782G>A (p.(Leu594=))
ISCN -
DB-ID TLL1_000012 See all 3 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) 0.00064 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TLL1 NM_001204760.1 -?/. - c.*26772G>A r.(=) p.(=)


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