Variant #0000275166 (NC_000019.9:g.55671337C>T, NM_000363.4:c.-2380G>A (TNNI3))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.55671337C>T
DNA change (hg38) g.55159969=
Published as DNAAF3(NM_001256714.1):c.1294G>A (p.D432N), DNAAF3(NM_001256716.2):c.931G>A (p.D311N)
ISCN -
DB-ID DNAAF3_000007 See all 2 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 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 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.-2380G>A r.(?) p.(=)
DNAAF3 NM_001256715.1 -/. - c.1093= r.(=) p.(Asn365=)
DNAAF3 NM_178837.4 -/. - c.1234= r.(=) p.(Asn412=)


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