Variant #0000309267 (NC_000003.11:g.52485416C>T, NM_003280.2:c.445G>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.52485416C>T
DNA change (hg38) g.52451400C>T
Published as TNNC1(NM_003280.2):c.445G>A (p.D149N), TNNC1(NM_003280.3):c.445G>A (p.D149N)
ISCN -
DB-ID TNNC1_000006 See all 5 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +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.445G>A r.(?) p.(Asp149Asn)
NISCH NM_007184.3 ?/. - c.-4242C>T r.(?) p.(=)


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