Variant #0001024363 (NC_000002.11:g.179482533G>T, NM_001267550.1:c.47545C>A (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.179482533G>T
DNA change (hg38) -
Published as TTN(NM_001256850.1):c.42622C>A (p.(Pro14208Thr)), TTN(NM_001267550.1):c.47545C>A (p.P15849T), TTN(NM_001267550.2):c.47545C>A (p.P15849T)
ISCN -
DB-ID TTN_000244 See all 7 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) 0.00372 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2025-02-07 18:57:27 +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.47545C>A r.(?) p.(Pro15849Thr)


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