Variant #0000857898 (NC_000002.11:g.179399936G>C, NM_001267550.1:c.101406C>G (TTN))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.179399936G>C
DNA change (hg38) -
Published as TTN(NM_001256850.1):c.96483C>G (p.(Val32161=)), TTN(NM_001267550.1):c.101406C>G (p.V33802=), TTN(NM_001267550.2):c.101406C>G (p.V33802=)
ISCN -
DB-ID TTN_000236 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) 0.00368 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 2022-05-09 15:51:19 +02:00 (CEST)
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.101406C>G r.(?) p.(Val33802=)
TTN-AS1 NR_038272.1 -?/. - n.220-523G>C r.(?) -


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