Variant #0000925868 (NC_000014.8:g.24710467_24710468insTGATC, NM_001099274.1:c.450_451insATCAG (TINF2))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.24710467_24710468insTGATC
DNA change (hg38) -
Published as TINF2(NM_001099274.3):c.450_451insATCAG (p.L151Ifs*26)
ISCN -
DB-ID GMPR2_000020
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +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     
TINF2 NM_001099274.1 +?/. - c.450_451insATCAG r.(?) p.(Leu151Ilefs*26)
GMPR2 NM_016576.3 +?/. - c.*2483_*2484insTGATC r.(=) p.(=)


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