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mutation t@sting

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Prediction

disease causing

Model: without_aae, prob: 0.999999999992581      (explain)
Summary
  • known disease mutation at this position (HGMD CM098498)
  • protein features (might be) affected
  • splice site changes
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr18:57134052G>AN/A show variant in all transcripts   IGV
HGNC symbol CCBE1
Ensembl transcript ID ENST00000398179
Genbank transcript ID N/A
UniProt peptide Q6UXH8
alteration type single base exchange
alteration region 5'UTR
DNA changes cDNA.262C>T
g.230561C>T
AA changes N/A
position(s) of altered AA
if AA alteration in CDS
N/A
frameshift N/A
known variant Reference ID: rs121908253
databasehomozygous (A/A)heterozygousallele carriers
1000G011
ExAC02727

known disease mutation at this position, please check HGMD for details (HGMD ID CM098498)

known disease mutation at this position, please check HGMD for details (HGMD ID CM098498)
known disease mutation at this position, please check HGMD for details (HGMD ID CM098498)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)2.5081
0.4641
(flanking)2.6071
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites splice site change before start ATG (at aa -63) |
effectgDNA positionscoredetection sequence  exon-intron border
Acc increased230568wt: 0.49 / mu: 0.61wt: CTTGGGCAGCTACCGCTGCGAGTGCCGGGAAGGCTACATCC
mu: CTTGGGCAGCTACTGCTGCGAGTGCCGGGAAGGCTACATCC
 gcga|GTGC
Donor marginally increased230563wt: 0.9123 / mu: 0.9295 (marginal change - not scored)wt: TACCGCTGCGAGTGC
mu: TACTGCTGCGAGTGC
 CCGC|tgcg
distance from splice site 72
Kozak consensus sequence altered? no
conservation
protein level for non-synonymous changes
N/A
protein features
start (aa)end (aa)featuredetails 
134SIGNALPotential.might get lost (downstream of altered splice site)
134175DOMAINEGF-like; calcium-binding (Potential).might get lost (downstream of altered splice site)
138138DISULFIDBy similarity.might get lost (downstream of altered splice site)
142142CARBOHYDN-linked (GlcNAc...) (Potential).might get lost (downstream of altered splice site)
146146DISULFIDBy similarity.might get lost (downstream of altered splice site)
150150DISULFIDBy similarity.might get lost (downstream of altered splice site)
159159DISULFIDBy similarity.might get lost (downstream of altered splice site)
161161DISULFIDBy similarity.might get lost (downstream of altered splice site)
174174DISULFIDBy similarity.might get lost (downstream of altered splice site)
182182CARBOHYDN-linked (GlcNAc...) (Potential).might get lost (downstream of altered splice site)
245290DOMAINCollagen-like 1.might get lost (downstream of altered splice site)
300333DOMAINCollagen-like 2.might get lost (downstream of altered splice site)
length of protein N/A
AA sequence altered N/A
position of stopcodon in wt / mu CDS N/A
position (AA) of stopcodon in wt / mu AA sequence N/A
position of stopcodon in wt / mu cDNA N/A
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now
N/A
position of start ATG in wt / mu cDNA 464 / 464
chromosome 18
strand -1
last intron/exon boundary 638
theoretical NMD boundary in CDS 124
length of CDS 408
coding sequence (CDS) position N/A
cDNA position
(for ins/del: last normal base / first normal base)
262
gDNA position
(for ins/del: last normal base / first normal base)
230561
chromosomal position
(for ins/del: last normal base / first normal base)
57134052
original gDNA sequence snippet TCAATACCTTGGGCAGCTACCGCTGCGAGTGCCGGGAAGGC
altered gDNA sequence snippet TCAATACCTTGGGCAGCTACTGCTGCGAGTGCCGGGAAGGC
original cDNA sequence snippet TCAATACCTTGGGCAGCTACCGCTGCGAGTGCCGGGAAGGC
altered cDNA sequence snippet TCAATACCTTGGGCAGCTACTGCTGCGAGTGCCGGGAAGGC
wildtype AA sequence MQLTWASISL VTRCWPQTPT FQDLLACLGA RALPGPPGAP GRDGSKGERG APGPRGSPGP
PGSFDFLLLM LADIRNDITE LQEKVFGHRT HSSAEEFPLP QEFPSYPEAM DLGSGDDHPR
RTETRDLRAP RDFYP*
mutated AA sequence N/A
speed 0.42 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project