Variant #0000552444 (NC_000014.8:g.24709952G>T, NM_001099274.1:c.734C>A (TINF2))

Chromosome 14
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.24709952G>T
DNA change (hg38) g.24240746G>T
Published as TINF2(NM_001099274.1):c.734C>A (p.(Ser245Tyr)), TINF2(NM_001099274.3):c.734C>A (p.S245Y), TINF2(NM_012461.2):c.734C>A (p.S245Y), TINF2(NM_012461.3)...
ISCN -
DB-ID TINF2_000003 See all 5 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) 0.00114 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TINF2 NM_001099274.1 ?/. - c.734C>A r.(?) p.(Ser245Tyr)
GMPR2 NM_016576.3 ?/. - c.*1968G>T r.(=) p.(=)


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