Variant #0000925534 (NC_000012.11:g.111066669A>G, NM_024549.5:c.570A>G (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.111066669A>G
DNA change (hg38) -
Published as TCTN1(NM_001082538.3):c.570A>G (p.E190=), TCTN1(NM_001319681.1):c.36A>G (p.E12=)
ISCN -
DB-ID TCTN1_000005 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) 0.00012 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 2023-04-16 21:50:28 +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.570A>G r.(?) p.(Glu190=)
TCTN1 NM_024549.5 -?/. - c.570A>G r.(?) p.(Glu190=)
HVCN1 NM_032369.3 -?/. - c.*20546T>C r.(=) p.(=)


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