Variant #0000248117 (NC_000002.11:g.179664441A>G, NM_001267550.1:c.687T>C (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.179664441A>G
DNA change (hg38) g.178799714A>G
Published as TTN(NM_001256850.1):c.687T>C (p.(Phe229=)), TTN(NM_001267550.1):c.687T>C (p.F229=), TTN(NM_001267550.2):c.687T>C (p.F229=), TTN(NM_133432.3):c.687T...
ISCN -
DB-ID TTN_003539 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) 0.00018 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 2018-01-15 20:58:59 +01:00 (CET)
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.687T>C r.(?) p.(Phe229=)
TTN NM_133379.3 -?/. - c.687T>C r.(?) p.(Phe229=)


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