Variant #0000991937 (NC_000002.11:g.179424835G>A, NM_001267550.1:c.86024C>T (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.179424835G>A
DNA change (hg38) -
Published as TTN(NM_001267550.1):c.86024C>T (p.P28675L, p.(Pro28675Leu))
ISCN -
DB-ID TTN_003699 See all 3 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) 2.0E-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 2024-08-28 13:07:21 +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     
TTN NM_001267550.1 ?/. - c.86024C>T r.(?) p.(Pro28675Leu)
TTN-AS1 NR_038272.1 ?/. - n.2043+17747G>A r.(?) -


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