Variant #0000991855 (NC_000002.11:g.179392469A>G, NM_001267550.1:c.107384T>C (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.179392469A>G
DNA change (hg38) -
Published as TTN(NM_001256850.1):c.102461T>C (p.(Val34154Ala)), TTN(NM_001267550.2):c.107384T>C (p.V35795A)
ISCN -
DB-ID TTN_001054 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) 6.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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.107384T>C r.(?) p.(Val35795Ala)
TTN-AS1 NR_038272.1 ?/. - n.219+4106A>G r.(?) -


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