Variant #0000853820 (NC_000014.8:g.24709057G>A, NM_001099274.1:c.1302C>T (TINF2))

Chromosome 14
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.24709057G>A
DNA change (hg38) -
Published as TINF2(NM_001099274.1):c.1302C>T (p.H434=), TINF2(NM_001099274.3):c.1302C>T (p.H434=)
ISCN -
DB-ID GMPR2_000009 See all 2 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) 8.0E-5 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 2022-05-09 15:40:45 +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.1302C>T r.(?) p.(His434=)
GMPR2 NM_016576.3 -?/. - c.*1073G>A r.(=) p.(=)


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