Variant #0000857595 (NC_000001.10:g.74701182A>G, NC_000001.10(NM_015978.2):c.40+7A>G (TNNI3K))

Chromosome 1
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.74701182A>G
DNA change (hg38) -
Published as TNNI3K(NM_015978.3):c.40+7A>G
ISCN -
DB-ID FPGT-TNNI3K_000104
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 15:51:19 +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     
FPGT-TNNI3K NM_001112808.2 -?/. - c.383-604A>G r.(=) p.(=)
TNNI3K NM_015978.2 -?/. - c.40+7A>G r.(=) p.(=)


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