Variant #0000983659 (NC_000019.9:g.55671257C>A, NM_000363.4:c.-2300G>T (TNNI3))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.55671257C>A
DNA change (hg38) -
Published as DNAAF3(NM_001256714.1):c.1364+10G>T, DNAAF3(NM_001256715.2):c.1163+10G>T
ISCN -
DB-ID DNAAF3_000006 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) 0.00229 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNNI3 NM_000363.4 -?/. - c.-2300G>T r.(?) p.(=)
DNAAF3 NM_001256715.1 -?/. - c.1163+10G>T r.(=) p.(=)
DNAAF3 NM_178837.4 -?/. - c.1304+10G>T r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.