Variant #0000883062 (NC_000001.10:g.201331511C>T, NC_000001.10(NM_001001430.2):c.579+3G>A (TNNT2))

Chromosome 1
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.201331511C>T
DNA change (hg38) -
Published as TNNT2(NM_001001430.3):c.579+3G>A
ISCN -
DB-ID TNNT2_000318
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:01:21 +01:00 (CET)
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.579+3G>A r.spl? p.?
TNNT2 NM_001276345.2 -?/. - c.609+3G>A r.spl? p.?


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