Variant #0000513600 (NC_000002.11:g.179666894G>C, NM_001267550.1:c.266C>G (TTN))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.179666894G>C
DNA change (hg38) g.178802167G>C
Published as TTN(NM_001267550.1):c.266C>G (p.(Ala89Gly)), TTN(NM_001267550.2):c.266C>G (p.A89G)
ISCN -
DB-ID TTN_005406 See all 3 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) 0.00013 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:07:21 +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.266C>G r.(?) p.(Ala89Gly)
TTN NM_133379.3 ?/. - c.266C>G r.(?) p.(Ala89Gly)


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