Transcript | Gene symbol | Prediction | Tree vote | Model | Prediction problem | Splice site change | Known ClinVar disease mutation | Potential ClinVar disease mutation | Amino acid changes | Variant type | dbSNP ID | Protein length | Features at a glance |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ENST00000216115(MANE Select) | BIK | Benign | 39|61 | simple_ | No | Single base exchange | Normal |
|
Analysed issue | Analysis result | |||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Variant | Chr22:43128525C>G (GRCh38) | |||||||||||||
Gene symbol | BIK | |||||||||||||
Gene constraints | LOEUF: 1.84, LOF (oe): 1.27, misssense (oe): 1.11, synonymous (oe): 1.11 (gnomAD) | |||||||||||||
Ensembl transcript ID | ENST00000216115.3 | |||||||||||||
Genbank transcript ID | NM_001197 (exact from MANE) | |||||||||||||
UniProt / AlphaMissense peptide | BIK_HUMAN | AlphaMissense: transcript, gene | |||||||||||||
Variant type | Single base exchange | |||||||||||||
Gene region | CDS | |||||||||||||
DNA changes | c.290C>G g.17776C>G | |||||||||||||
AA changes |
| |||||||||||||
Frameshift | No | |||||||||||||
Length of protein | Normal | |||||||||||||
Pathogenic variant (ClinVar) | Variant not listed in ClinVar as (likely) pathogenic. | |||||||||||||
Variant DBs |
| |||||||||||||
Protein conservation | ||||||||||||||
Protein features |
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Phylogenetic conservation |
| |||||||||||||
Splice sites | No abrogation of potential splice sites predicted by MaxEntScan. | |||||||||||||
Distance from splice site | N/A | |||||||||||||
Kozak consensus sequence altered? | No | |||||||||||||
poly(A) signal | N/A | |||||||||||||
AA sequence altered | Yes | |||||||||||||
Chromosome | 22 | |||||||||||||
Strand | 1 | |||||||||||||
Original gDNA sequence snippet | GGCTTTCATCTACGACCAGACTGAGGACATCAGGGATGTTC | |||||||||||||
Altered gDNA sequence snippet | GGCTTTCATCTACGACCAGAGTGAGGACATCAGGGATGTTC | |||||||||||||
Original cDNA sequence snippet | GGCTTTCATCTACGACCAGACTGAGGACATCAGGGATGTTC | |||||||||||||
Altered cDNA sequence snippet | GGCTTTCATCTACGACCAGAGTGAGGACATCAGGGATGTTC | |||||||||||||
Wildtype AA sequence | MSEVRPLSRD ILMETLLYEQ LLEPPTMEVL GMTDSEEDLD PMEDFDSLEC MEGSDALALR LACIGDEMDV SLRAPRLAQL SEVAMHSLGL AFIYDQTEDI RDVLRSFMDG FTTLKENIMR FWRSPNPGSW VSCEQVLLAL LLLLALLLPL LSGGLHLLLK * | |||||||||||||
Mutated AA sequence | MSEVRPLSRD ILMETLLYEQ LLEPPTMEVL GMTDSEEDLD PMEDFDSLEC MEGSDALALR LACIGDEMDV SLRAPRLAQL SEVAMHSLGL AFIYDQSEDI RDVLRSFMDG FTTLKENIMR FWRSPNPGSW VSCEQVLLAL LLLLALLLPL LSGGLHLLLK * | |||||||||||||
Position of stopcodon in wt / mu CDS | 483 / 483 | |||||||||||||
Position (AA) of stopcodon in wt / mu AA sequence | 161 / 161 | |||||||||||||
Position of stopcodon in wt / mu cDNA | 544 / 544 | |||||||||||||
Position of start ATG in wt / mu cDNA | 62 / 62 | |||||||||||||
Last intron/exon boundary | 451 | |||||||||||||
Theoretical NMD boundary in CDS | 339 | |||||||||||||
Length of CDS | 483 | |||||||||||||
Coding sequence (CDS) position | 290 | |||||||||||||
cDNA position | 351 | |||||||||||||
gDNA position | 17776 | |||||||||||||
Chromosomal position | 43128525 | |||||||||||||
Speed | 0.35 s |
All positions are in basepairs (bp) if not explicitly stated differently. cDNA/gDNA/chromosomal position: Ins/del are shown as 'last normal base / first normal base'.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project