Variant #0000543349 (NC_000011.9:g.1862244G>A, NC_000011.9(NM_003282.3):c.277-17G>A (TNNI2))

Chromosome 11
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.1862244G>A
DNA change (hg38) g.1841014G>A
Published as TNNI2(NM_001145829.2):c.277-17G>A
ISCN -
DB-ID SYT8_000010
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) 0.00345 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNNI2 NM_003282.3 -/. - c.277-17G>A r.(=) p.(=)
SYT8 NM_138567.3 -/. - c.*3583G>A r.(=) p.(=)


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