Variant #0000327993 (NC_000002.11:g.179664633_179664635del, NM_001267550.1:c.593_595del (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.179664633_179664635del
DNA change (hg38) g.178799906_178799908del
Published as TTN(NM_001256850.1):c.593_595del (p.?), TTN(NM_001267550.1):c.593_595delAAG (p.E198del), TTN(NM_001267550.2):c.593_595delAAG (p.E198del)
ISCN -
DB-ID TTN_003545 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTN NM_001267550.1 ?/. - c.593_595del r.(?) p.(Glu198del)
TTN NM_133379.3 ?/. - c.593_595del r.(?) p.(Glu198del)


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