Variant #0000606436 (NC_000002.11:g.179401935C>T, NM_001267550.1:c.99901G>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.179401935C>T
DNA change (hg38) g.178537208C>T
Published as TTN(NM_001256850.1):c.94978G>A (p.(Glu31660Lys)), TTN(NM_001267550.1):c.99901G>A (p.E33301K), TTN(NM_001267550.2):c.99901G>A (p.E33301K), TTN(NM_1...)
ISCN -
DB-ID TTN_000993 See all 11 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) 0.00029 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 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.99901G>A r.(?) p.(Glu33301Lys)
TTN-AS1 NR_038272.1 -?/. - n.317-153C>T r.(?) -


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