Variant #0000546496 (NC_000012.11:g.111066587C>A, NM_024549.5:c.488C>A (TCTN1))

Chromosome 12
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.111066587C>A
DNA change (hg38) g.110628782C>A
Published as TCTN1(NM_024549.6):c.488C>A (p.S163Y)
ISCN -
DB-ID TCTN1_000019 See all 2 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) 0.00245 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.488C>A r.(?) p.(Ser163Tyr)
TCTN1 NM_024549.5 -/. - c.488C>A r.(?) p.(Ser163Tyr)
HVCN1 NM_032369.3 -/. - c.*20628G>T r.(=) p.(=)


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