Variant #0000355120 (NC_000001.10:g.201328373G>A, NM_001001430.2:c.832C>T (TNNT2))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.201328373G>A
DNA change (hg38) g.201359245G>A
Published as Arg278Cys
ISCN -
DB-ID TNNT2_000007 See all 33 reported entries
Variant remarks expression cloning no Ca2+–sensitizing effect
Reference {PMID10085122:Yanaga 1999}
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00036 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2011-07-02 22:11:33 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNNT2 NM_001001430.2 ?/. 16 c.832C>T r.(?) p.Arg278Cys


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