Variant #0000678967 (NC_000010.10:g.97445336T>C, NM_015631.5:c.946A>G (TCTN3))

Chromosome 10
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.97445336T>C
DNA change (hg38) -
Published as TCTN3(NM_015631.5):c.946A>G (p.T316A, p.(Thr316Ala)), TCTN3(NM_015631.6):c.946A>G (p.T316A)
ISCN -
DB-ID TCTN3_000028 See all 3 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) 0.00082 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TCTN3 NM_015631.5 -?/. - c.946A>G r.(?) p.(Thr316Ala)


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