Variant #0000923046 (NC_000001.10:g.201328345C>T, NM_001001430.2:c.860G>A (TNNT2))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.201328345C>T
DNA change (hg38) -
Published as TNNT2(NM_000364.4):c.881G>A (p.W294*), TNNT2(NM_001276347.2):c.860G>A (p.W287*)
ISCN -
DB-ID TNNT2_000084 See all 4 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-04-16 21:50:28 +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     
TNNT2 NM_001001430.2 +?/. - c.860G>A r.(?) p.(Trp287Ter)


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