Variant #0000883057 (NC_000001.10:g.201328386G>A, NC_000001.10(NM_001001430.2):c.822-3C>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.201328386G>A
DNA change (hg38) -
Published as TNNT2(NM_001276347.2):c.822-3C>T
ISCN -
DB-ID TNNT2_000313
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
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.822-3C>T r.spl? p.?
TNNT2 NM_001276345.2 ?/. - c.852-3C>T r.spl? p.?


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