Variant #0000311856 (NC_000014.8:g.24711465C>G, NM_001099274.1:c.74G>C (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.24711465C>G
DNA change (hg38) g.24242259C>G
Published as TINF2(NM_012461.2):c.74G>C (p.G25A), TINF2(NM_012461.3):c.74G>C (p.G25A)
ISCN -
DB-ID TINF2_000032 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) 0.00177 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.74G>C r.(?) p.(Gly25Ala)
GMPR2 NM_016576.3 -/. - c.*3481C>G r.(=) p.(=)


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