Variant #0001038937 (NC_000012.11:g.111054083G>T, NC_000012.11(NM_024549.5):c.220+1876G>T (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.111054083G>T
DNA change (hg38) -
Published as TCTN1(NM_001173976.2):c.-35G>T
ISCN -
DB-ID TCTN1_000044
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) 4.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
TCTN1 NM_001082538.2 -?/. - c.220+1876G>T r.(=) p.(=)
TCTN1 NM_024549.5 -?/. - c.220+1876G>T r.(=) p.(=)
HVCN1 NM_032369.3 -?/. - c.*33132C>A r.(=) p.(=)


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