Variant #0000520380 (NC_000003.11:g.52486216G>T, NM_003280.2:c.108C>A (TNNC1))

Chromosome 3
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.52486216G>T
DNA change (hg38) g.52452200G>T
Published as TNNC1(NM_003280.2):c.108C>A (p.I36=), TNNC1(NM_003280.3):c.108C>A (p.I36=)
ISCN -
DB-ID TNNC1_000024 See all 3 reported entries
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) 0.00056 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNNC1 NM_003280.2 -?/. - c.108C>A r.(?) p.(Ile36=)
NISCH NM_007184.3 -?/. - c.-3442G>T r.(?) p.(=)


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