Variant #0001046469 (NC_000014.8:g.24709506C>T, NM_001099274.1:c.1092G>A (TINF2))

Chromosome 14
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.24709506C>T
DNA change (hg38) -
Published as TINF2(NM_001099274.1):c.1092G>A (p.L364=, p.(Leu364=))
ISCN -
DB-ID TINF2_000035 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) 0.00551 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2025-07-08 13:22:38 +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.1092G>A r.(?) p.(Leu364=)
GMPR2 NM_016576.3 -/. - c.*1522C>T r.(=) p.(=)


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