Variant #0000952547 (NC_000002.11:g.179489191C>T, NC_000002.11(NM_001267550.1):c.44815+1G>A (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.179489191C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID TTN_005415 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1274007753
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-12-11 14:45:01 +01:00 (CET)
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.44815+1G>A r.(?) p.(?)


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