Variant #0000511349 (NC_000002.11:g.179438480C>T, NM_001267550.1:c.72379G>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.179438480C>T
DNA change (hg38) g.178573753C>T
Published as TTN(NM_001267550.1):c.72379G>A (p.E24127K), TTN(NM_001267550.2):c.72379G>A (p.E24127K, p.(Glu24127Lys))
ISCN -
DB-ID TTN_001734 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) 0.00042 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 2024-04-19 20:20:39 +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.72379G>A r.(?) p.(Glu24127Lys)
TTN-AS1 NR_038272.1 -?/. - n.2044-8819C>T r.(?) -


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