Variant #0000321913 (NC_000011.9:g.1857712C>A, NM_003282.3:c.-2574C>A (TNNI2))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.1857712C>A
DNA change (hg38) g.1836482C>A
Published as SYT8(NM_138567.3):c.616C>A (p.(Arg206Ser))
ISCN -
DB-ID SYT8_000003
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) 0.0001 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.-2574C>A r.(?) p.(=)
SYT8 NM_138567.3 ?/. - c.616C>A r.(?) p.(Arg206Ser)


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