Variant #0000329447 (NC_000003.11:g.52486507T>C, NM_003280.2:c.47A>G (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.52486507T>C
DNA change (hg38) g.52452491T>C
Published as TNNC1(NM_003280.2):c.47A>G (p.(Gln16Arg))
ISCN -
DB-ID TNNC1_000027
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.47A>G r.(?) p.(Gln16Arg)
NISCH NM_007184.3 +?/. - c.-3151T>C r.(?) p.(=)


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