Variant #0000885931 (NC_000003.11:g.52485426G>T, NM_003280.2:c.435C>A (TNNC1))

Chromosome 3
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.52485426G>T
DNA change (hg38) -
Published as TNNC1(NM_003280.3):c.435C>A (p.D145E)
ISCN -
DB-ID NISCH_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) 0.00013 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-11-01 13:01:21 +01:00 (CET)
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.435C>A r.(?) p.(Asp145Glu)
NISCH NM_007184.3 ?/. - c.-4232G>T r.(?) p.(=)


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