Variant #0000923049 (NC_000001.10:g.201338973T>A, NC_000001.10(NM_001001430.2):c.68-1618A>T (TNNT2))

Chromosome 1
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.201338973T>A
DNA change (hg38) -
Published as TNNT2(NM_001276345.2):c.68A>T (p.E23V)
ISCN -
DB-ID TNNT2_000329
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNNT2 NM_001001430.2 ?/. - c.68-1618A>T r.(=) p.(=)
TNNT2 NM_001276345.2 ?/. - c.68A>T r.(?) p.(Glu23Val)


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