Variant #0000310873 (NC_000002.11:g.179632598C>T, NM_001267550.1:c.9359G>A (TTN))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.179632598C>T
DNA change (hg38) g.178767871C>T
Published as TTN(NM_001256850.1):c.9359G>A (p.(Arg3120Gln)), TTN(NM_001267550.1):c.9359G>A (p.R3120Q), TTN(NM_001267550.2):c.9359G>A (p.R3120Q)
ISCN -
DB-ID TTN_000629 See all 8 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) 0.00419 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTN NM_001267550.1 -/. - c.9359G>A r.(?) p.(Arg3120Gln)
TTN NM_133379.3 -/. - c.9359G>A r.(?) p.(Arg3120Gln)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.