Variant #0000888329 (NC_000008.10:g.33370001_33370002del, NM_025115.3:c.130_131del (TTI2))

Chromosome 8
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.33370001_33370002del
DNA change (hg38) -
Published as TTI2(NM_025115.3):c.130_131delCG (p.G45Qfs*8)
ISCN -
DB-ID MAK16_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) 0.0001 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
TTI2 NM_025115.3 ?/. - c.130_131del r.(?) p.(Gly45Glnfs*8)
MAK16 NM_032509.3 ?/. - c.*13854_*13855del r.(=) p.(=)


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