Variant #0000800165 (NC_000002.11:g.179610967C>T, NC_000002.11(NM_001267550.1):c.11312-4319G>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.179610967C>T
DNA change (hg38) -
Published as TTN(NM_133379.3):c.16160G>A (p.(Cys5387Tyr)), TTN(NM_133379.4):c.16160G>A (p.C5387Y), TTN(NM_133379.5):c.16160G>A (p.C5387Y)
ISCN -
DB-ID TTN_000865 See all 9 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) 0.00305 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTN NM_001267550.1 -?/. - c.11312-4319G>A r.(=) p.(=)
TTN NM_133379.3 -?/. - c.16160G>A r.(?) p.(Cys5387Tyr)


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