Variant #0000947456 (NC_000002.11:g.179417638A>T, NM_001267550.1:c.89989T>A (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.179417638A>T
DNA change (hg38) -
Published as TTN(NM_001256850.1):c.85066T>A (p.(Leu28356Met)), TTN(NM_001267550.1):c.89989T>A (p.L29997M), TTN(NM_001267550.2):c.89989T>A (p.L29997M)
ISCN -
DB-ID TTN_000969 See all 5 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) 0.00146 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 2023-11-27 17:35:39 +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.89989T>A r.(?) p.(Leu29997Met)
TTN-AS1 NR_038272.1 -/. - n.2043+10550A>T r.(?) -


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