Variant #0000316857 (NC_000019.9:g.55665456T>G, NM_000363.4:c.491A>C (TNNI3))

Chromosome 19
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.55665456T>G
DNA change (hg38) g.55154088T>G
Published as TNNI3(NM_000363.4):c.491A>C (p.K164T), TNNI3(NM_000363.5):c.491A>C (p.K164T)
ISCN -
DB-ID TNNI3_000069 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNNI3 NM_000363.4 ?/. - c.491A>C r.(?) p.(Lys164Thr)
DNAAF3 NM_001256715.1 ?/. - c.*4974A>C r.(=) p.(=)
TNNT1 NM_003283.4 ?/. - c.-4939A>C r.(?) p.(=)
DNAAF3 NM_178837.4 ?/. - c.*4974A>C r.(=) p.(=)


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