Variant #0001000946 (NC_000014.8:g.24709259T>C, NC_000014.8(NM_001099274.1):c.1221+11A>G (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.24709259T>C
DNA change (hg38) -
Published as TINF2(NM_012461.2):c.*362A>G (p.?)
ISCN -
DB-ID GMPR2_000024
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 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 2024-08-28 13:16:32 +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.1221+11A>G r.(=) p.(=)
GMPR2 NM_016576.3 -?/. - c.*1275T>C r.(=) p.(=)


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