Variant #0000911432 (NC_000002.11:g.179606288G>A, NM_001267550.1:c.11672C>T (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.179606288G>A
DNA change (hg38) -
Published as TTN(NM_001267550.1):c.11672C>T (p.T3891I), TTN(NM_001267550.2):c.11672C>T (p.T3891I)
ISCN -
DB-ID TTN_003154 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) 0.00044 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +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.11672C>T r.(?) p.(Thr3891Ile)
TTN NM_133379.3 -?/. - c.*4024C>T r.(=) p.(=)


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