Variant #0000925356 (NC_000011.9:g.1862317A>G, NM_003282.3:c.333A>G (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.1862317A>G
DNA change (hg38) -
Published as TNNI2(NM_001145829.2):c.333A>G (p.P111=)
ISCN -
DB-ID SYT8_000012
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) 0.00075 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNNI2 NM_003282.3 -?/. - c.333A>G r.(?) p.(Pro111=)
SYT8 NM_138567.3 -?/. - c.*3656A>G r.(=) p.(=)


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