Variant #0000723354 (NC_000011.9:g.1861691G>C, NC_000011.9(NM_003282.3):c.57+17G>C (TNNI2))

Chromosome 11
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.1861691G>C
DNA change (hg38) -
Published as TNNI2(NM_001145829.2):c.57+17G>C
ISCN -
DB-ID SYT8_000011 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) 0.0005 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNNI2 NM_003282.3 -?/. - c.57+17G>C r.(=) p.(=)
SYT8 NM_138567.3 -?/. - c.*3030G>C r.(=) p.(=)


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