Variant #0000679395 (NC_000012.11:g.111080092T>C, NM_024549.5:c.1187T>C (TCTN1))

Chromosome 12
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.111080092T>C
DNA change (hg38) -
Published as TCTN1(NM_001319681.1):c.695T>C (p.L232P)
ISCN -
DB-ID TCTN1_000027
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_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 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.1229T>C r.(?) p.(Leu410Pro)
TCTN1 NM_024549.5 ?/. - c.1187T>C r.(?) p.(Leu396Pro)
HVCN1 NM_032369.3 ?/. - c.*7123A>G r.(=) p.(=)


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