| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ENST00000312150(MANE Select) | KRT25 | Benign | 0|100 | 3utr | No | Single base exchange | N/A |
|
| Analysed issue | Analysis result | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Variant | Chr17:40748150A>G (GRCh38) | |||||||||||||
| Gene symbol | KRT25 | |||||||||||||
| Gene constraints | LOEUF: 1.00, LOF (oe): 0.75, misssense (oe): 0.93, synonymous (oe): 0.93 (gnomAD) | |||||||||||||
| Ensembl transcript ID | ENST00000312150.5 | |||||||||||||
| Genbank transcript ID | NM_181534 (exact from MANE) | |||||||||||||
| UniProt / AlphaMissense peptide | N/A | |||||||||||||
| Variant type | Single base exchange | |||||||||||||
| Gene region | 3'UTR | |||||||||||||
| DNA changes | cDNA.1540T>C g.7182T>C | |||||||||||||
| AA changes | N/A | |||||||||||||
| Frameshift | No | |||||||||||||
| Length of protein | N/A | |||||||||||||
| Pathogenic variant (ClinVar) | Variant not listed in ClinVar as (likely) pathogenic. | |||||||||||||
| Variant DBs |
| |||||||||||||
| Protein conservation | N/A | |||||||||||||
| Protein features | N/A | |||||||||||||
| Phylogenetic conservation |
| |||||||||||||
| Splice sites | No abrogation of potential splice sites predicted by MaxEntScan. | |||||||||||||
| Distance from splice site | N/A | |||||||||||||
| Kozak consensus sequence altered? | N/A | |||||||||||||
| poly(A) signal | polyA signal ok | |||||||||||||
| AA sequence altered | N/A | |||||||||||||
| Chromosome | 17 | |||||||||||||
| Strand | -1 | |||||||||||||
| Original gDNA sequence snippet | TCTTTCTGTTACTTTCTTTCTGGGCAATCAATGACAGCATC | |||||||||||||
| Altered gDNA sequence snippet | TCTTTCTGTTACTTTCTTTCCGGGCAATCAATGACAGCATC | |||||||||||||
| Original cDNA sequence snippet | TCTTTCTGTTACTTTCTTTCTGGGCAATCAATGACAGCATC | |||||||||||||
| Altered cDNA sequence snippet | TCTTTCTGTTACTTTCTTTCCGGGCAATCAATGACAGCATC | |||||||||||||
| Wildtype AA sequence | MSLRLSSASR RSCPRPTTGS LRLYGGGTSF GTGNSCGISG IGSGFSSAFG GSSSGGNTGG GNPCAGFTVN ERGLLSGNEK VTMQNLNDRL ASYLDSVHAL EEANADLEQK IKGWYEKFGP GSCRGLDHDY SRYFPIIDDL KNQIIASTTS NANAVLQIDN ARLTADDFRL KYENELALHQ SVEADVNGLR RVLDEITLCR TDLEIQYETL SEEMTYLKKN HKEEMQVLQC AAGGNVNVEM NAAPGVDLTV LLNNMRAEYE ALAEQNRRDA EAWFNEKSAS LQQQISEDVG ATTSARNELT EMKRTLQTLE IELQSLLATK HSLECSLTET ESNYCAQLAQ IQAQIGALEE QLHQVRTETE GQKLEYEQLL DIKLHLEKEI ETYCLLIGGD DGACKSGGYK SKDYGSGNVG SQVKDPAKAI VVKKVLEEVD QRSKILTTRL HSLEEKSQSN * | |||||||||||||
| Mutated AA sequence | ||||||||||||||
| 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 | |||||||||||||
| Position of start ATG in wt / mu cDNA | 61 / 61 | |||||||||||||
| Last intron/exon boundary | 1303 | |||||||||||||
| Theoretical NMD boundary in CDS | 1192 | |||||||||||||
| Length of CDS | 1353 | |||||||||||||
| Coding sequence (CDS) position | N/A | |||||||||||||
| cDNA position | 1540 | |||||||||||||
| gDNA position | 7182 | |||||||||||||
| Chromosomal position | 40748150 | |||||||||||||
| Speed | 0.09 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