Variant #0000622782 (NC_000012.11:g.111072248G>A, NM_024549.5:c.760G>A (TCTN1))

Chromosome 12
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.111072248G>A
DNA change (hg38) g.110634443G>A
Published as TCTN1(NM_024549.5):c.760G>A (p.E254K)
ISCN -
DB-ID TCTN1_000024
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) 0.0023 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TCTN1 NM_001082538.2 -?/. - c.713-227G>A r.(=) p.(=)
TCTN1 NM_024549.5 -?/. - c.760G>A r.(?) p.(Glu254Lys)
HVCN1 NM_032369.3 -?/. - c.*14967C>T r.(=) p.(=)


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