Variant #0001046935 (NC_000002.11:g.179442784C>G, NM_001267550.1:c.68458G>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.179442784C>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID TTN_000832 See all 8 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs72646880
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00194 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-07-13 15:42:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTN NM_001267550.1 -/. - c.68458G>C r.(?) p.(Ala22820Pro)


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