Variant #0000316622 (NC_000014.8:g.24709075G>A, NM_001099274.1:c.1284C>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.24709075G>A
DNA change (hg38) g.24239869G>A
Published as TINF2(NM_001099274.1):c.1284C>T (p.Y428=)
ISCN -
DB-ID TINF2_000034
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) 1.0E-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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-05 13:46:33 +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.1284C>T r.(?) p.(Tyr428=)
GMPR2 NM_016576.3 -?/. - c.*1091G>A r.(=) p.(=)


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