Variant #0000520360 (NC_000003.11:g.52485425C>T, NM_003280.2:c.436G>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.52485425C>T
DNA change (hg38) g.52451409C>T
Published as TNNC1(NM_003280.2):c.436G>A (p.G146S), TNNC1(NM_003280.3):c.436G>A (p.G146S)
ISCN -
DB-ID NISCH_000004 See all 4 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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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.436G>A r.(?) p.(Gly146Ser)
NISCH NM_007184.3 ?/. - c.-4233C>T r.(?) p.(=)


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