Variant #0000511610 (NC_000002.11:g.179452695C>T, NM_001267550.1:c.63439G>A (TTN))

Chromosome 2
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.179452695C>T
DNA change (hg38) g.178587968C>T
Published as TTN(NM_001256850.1):c.58516G>A (p.(Ala19506Thr)), TTN(NM_001267550.1):c.63439G>A (p.A21147T), TTN(NM_001267550.2):c.63439G>A (p.A21147T)
ISCN -
DB-ID TTN_000588 See all 6 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) 0.0006 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 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     
TTN NM_001267550.1 ?/. - c.63439G>A r.(?) p.(Ala21147Thr)
TTN-AS1 NR_038272.1 ?/. - n.3188+2975C>T r.(?) -


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