Variant #0000510852 (NC_000002.11:g.179414800C>T, NM_001267550.1:c.91765G>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.179414800C>T
DNA change (hg38) g.178550073C>T
Published as TTN(NM_001256850.1):c.86842G>A (p.(Ala28948Thr)), TTN(NM_001267550.1):c.91765G>A (p.A30589T), TTN(NM_001267550.2):c.91765G>A (p.A30589T)
ISCN -
DB-ID TTN_000239 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) 0.00369 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTN NM_001267550.1 -?/. - c.91765G>A r.(?) p.(Ala30589Thr)
TTN-AS1 NR_038272.1 -?/. - n.2043+7712C>T r.(?) -


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