Variant #0000607332 (NC_000002.11:g.179669337C>T, NM_001267550.1:c.33G>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.179669337C>T
DNA change (hg38) g.178804610C>T
Published as TTN(NM_001267550.1):c.33G>A (p.(Pro11=)), TTN(NM_001267550.2):c.33G>A (p.P11=)
ISCN -
DB-ID TTN_003556 See all 4 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) 0.0002 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +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.33G>A r.(?) p.(Pro11=)
TTN NM_133379.3 -?/. - c.33G>A r.(?) p.(Pro11=)


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