Variant #0000511902 (NC_000002.11:g.179469764G>A, NM_001267550.1:c.54140C>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.179469764G>A
DNA change (hg38) g.178605037G>A
Published as TTN(NM_001267550.2):c.54140C>T (p.A18047V), TTN(NM_133432.3):c.27320C>T (p.A9107V)
ISCN -
DB-ID TTN_000838 See all 4 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) 3.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTN NM_001267550.1 ?/. - c.54140C>T r.(?) p.(Ala18047Val)
TTN-AS1 NR_038272.1 ?/. - n.4224G>A r.(?) -


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