Variant #0000789902 (NC_000003.11:g.52485826C>T, NM_003280.2:c.251G>A (TNNC1))

Chromosome 3
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.52485826C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID TNNC1_000036
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs267607126
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-06-21 11:42:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNNC1 NM_003280.2 +?/. - c.251G>A r.(?) p.(Cys84Tyr)


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