Variant #0000245706 (NC_000002.11:g.179444915A>G, NM_001267550.1:c.67099T>C (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.179444915A>G
DNA change (hg38) g.178580188A>G
Published as TTN(NM_001267550.1):c.67099T>C (p.S22367P), TTN(NM_001267550.2):c.67099T>C (p.S22367P, p.(Ser22367Pro)), TTN(NM_133432.3):c.40279T>C (p.S13427P)
ISCN -
DB-ID TTN_000213 See all 9 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) 0.00174 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 2024-04-19 20:20:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTN NM_001267550.1 -/. - c.67099T>C r.(?) p.(Ser22367Pro)
TTN-AS1 NR_038272.1 -/. - n.2044-2384A>G r.(?) -


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