Variant #0000318762 (NC_000002.11:g.179441148G>C, NC_000002.11(NM_001267550.1):c.69716-5C>G (TTN))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.179441148G>C
DNA change (hg38) g.178576421G>C
Published as TTN(NM_001256850.1):c.64793-5C>G (p.(=)), TTN(NM_001267550.1):c.69716-5C>G, TTN(NM_001267550.2):c.69716-5C>G, TTN(NM_133432.3):c.42896-5C>G, TTN-AS...
ISCN -
DB-ID TTN_000671 See all 8 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) 0.00266 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.69716-5C>G r.spl? p.?
TTN-AS1 NR_038272.1 -/. - n.2044-6151G>C r.(?) -


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