Yum, tasty mutations...

MutationTaster - study a chromosomal position

MTQE documentation
NEVER press reload or F5 - unless you want to start from the very beginning.
input seems to be ok - now mapping the variant to the different transcripts...
found 6 transcript(s)...
Querying Taster for transcript #1: ENST00000359758
Querying Taster for transcript #2: ENST00000361111
Querying Taster for transcript #3: ENST00000297498
Querying Taster for transcript #4: ENST00000458665
Querying Taster for transcript #5: ENST00000528168
Querying Taster for transcript #6: ENST00000398462
MT speed 8.72 s - this script 8.272684 s

Results


genesymbolpredictionprobabilitymodelprediction
problem
splicingClinVaramino acid changesvariant typedbSNP IDprotein lengthfile
SPAG11Bpolymorphism_automatic1.12021503184678e-13simple_aaeH84Rsingle base exchangers1042797show file
SPAG11Bpolymorphism_automatic1.12021503184678e-13simple_aaeH84Rsingle base exchangers1042797show file
SPAG11Bpolymorphism_automatic1.12021503184678e-13simple_aaeH31Rsingle base exchangers1042797show file
SPAG11Bpolymorphism_automatic1.48529510024531e-07without_aaesingle base exchangers1042797show file
SPAG11Bpolymorphism_automatic1.48529510024531e-07without_aaesingle base exchangers1042797show file
SPAG11Bpolymorphism_automatic1.48529510024531e-07without_aaesingle base exchangers1042797show file

Taster files

Yum, tasty mutations...

mutation t@sting

documentation

Prediction

polymorphism

Model: simple_aae, prob: 0.999999999999888 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr8:7308386T>CN/A show variant in all transcripts   IGV
HGNC symbol SPAG11B
Ensembl transcript ID ENST00000398462
Genbank transcript ID NM_058201
UniProt peptide Q08648
alteration type single base exchange
alteration region CDS
DNA changes c.251A>G
cDNA.402A>G
g.12811A>G
AA changes H84R Score: 29 explain score(s)
position(s) of altered AA
if AA alteration in CDS
84
frameshift no
known variant Reference ID: rs1042797
databasehomozygous (C/C)heterozygousallele carriers
1000G---
ExAC14826311517941
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-0.7340.005
-0.2930.01
(flanking)-0.1340.086
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc marginally increased12816wt: 0.2915 / mu: 0.2977 (marginal change - not scored)wt: GAAATACCATCTGCCATATGCAGCAAGGGATCTGCAGACTT
mu: GAAATACCATCTGCCGTATGCAGCAAGGGATCTGCAGACTT
 atgc|AGCA
distance from splice site 37
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      84DVPPGIRNTICHMQQGICRLFFCH
mutated  not conserved    84DVPPGIRNTICRMQQGICRLFFC
Ptroglodytes  not conserved  ENSPTRG00000019963  84DVPLGIRNTICRMQQGICRLFFC
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  not conserved  ENSMUSG00000059463  84EPEPNYQIVNCKKSEGQCQ-EYC
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
protein features no protein features affected
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 402 / 402
position (AA) of stopcodon in wt / mu AA sequence 134 / 134
position of stopcodon in wt / mu cDNA 553 / 553
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 152 / 152
chromosome 8
strand -1
last intron/exon boundary 366
theoretical NMD boundary in CDS 164
length of CDS 402
coding sequence (CDS) position 251
cDNA position
(for ins/del: last normal base / first normal base)
402
gDNA position
(for ins/del: last normal base / first normal base)
12811
chromosomal position
(for ins/del: last normal base / first normal base)
7308386
original gDNA sequence snippet AATTAGAAATACCATCTGCCATATGCAGCAAGGGATCTGCA
altered gDNA sequence snippet AATTAGAAATACCATCTGCCGTATGCAGCAAGGGATCTGCA
original cDNA sequence snippet AATTAGAAATACCATCTGCCATATGCAGCAAGGGATCTGCA
altered cDNA sequence snippet AATTAGAAATACCATCTGCCGTATGCAGCAAGGGATCTGCA
wildtype AA sequence MRQRLLPSVT SLLLVALLFP GSSQARHVNH SATEALGELR ERAPGQGTNG FQLLRHAVKR
DLLPPRTPPY QGDVPPGIRN TICHMQQGIC RLFFCHSGEK KRDICSDPWN RCCVSNTDEE
GKEKPEMDGR SGI*
mutated AA sequence MRQRLLPSVT SLLLVALLFP GSSQARHVNH SATEALGELR ERAPGQGTNG FQLLRHAVKR
DLLPPRTPPY QGDVPPGIRN TICRMQQGIC RLFFCHSGEK KRDICSDPWN RCCVSNTDEE
GKEKPEMDGR SGI*
speed 1.17 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
back to results table
Yum, tasty mutations...

mutation t@sting

documentation

Prediction

polymorphism

Model: simple_aae, prob: 0.999999999999888 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr8:7308386T>CN/A show variant in all transcripts   IGV
HGNC symbol SPAG11B
Ensembl transcript ID ENST00000359758
Genbank transcript ID NM_058200
UniProt peptide Q08648
alteration type single base exchange
alteration region CDS
DNA changes c.251A>G
cDNA.274A>G
g.12811A>G
AA changes H84R Score: 29 explain score(s)
position(s) of altered AA
if AA alteration in CDS
84
frameshift no
known variant Reference ID: rs1042797
databasehomozygous (C/C)heterozygousallele carriers
1000G---
ExAC14826311517941
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-0.7340.005
-0.2930.01
(flanking)-0.1340.086
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc marginally increased12816wt: 0.2915 / mu: 0.2977 (marginal change - not scored)wt: GAAATACCATCTGCCATATGCAGCAAGGGATCTGCAGACTT
mu: GAAATACCATCTGCCGTATGCAGCAAGGGATCTGCAGACTT
 atgc|AGCA
distance from splice site 37
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      84DVPPGIRNTICHMQQGICRLFFCH
mutated  not conserved    84DVPPGIRNTICRMQQGICRLFFC
Ptroglodytes  not conserved  ENSPTRG00000019963  84DVPLGIRNTICRMQQGICRLFFC
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  not conserved  ENSMUSG00000059463  84EPEPNYQIVNCKKSEGQCQ
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
protein features no protein features affected
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 327 / 327
position (AA) of stopcodon in wt / mu AA sequence 109 / 109
position of stopcodon in wt / mu cDNA 350 / 350
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 24 / 24
chromosome 8
strand -1
last intron/exon boundary 316
theoretical NMD boundary in CDS 242
length of CDS 327
coding sequence (CDS) position 251
cDNA position
(for ins/del: last normal base / first normal base)
274
gDNA position
(for ins/del: last normal base / first normal base)
12811
chromosomal position
(for ins/del: last normal base / first normal base)
7308386
original gDNA sequence snippet AATTAGAAATACCATCTGCCATATGCAGCAAGGGATCTGCA
altered gDNA sequence snippet AATTAGAAATACCATCTGCCGTATGCAGCAAGGGATCTGCA
original cDNA sequence snippet AATTAGAAATACCATCTGCCATATGCAGCAAGGGATCTGCA
altered cDNA sequence snippet AATTAGAAATACCATCTGCCGTATGCAGCAAGGGATCTGCA
wildtype AA sequence MRQRLLPSVT SLLLVALLFP GSSQARHVNH SATEALGELR ERAPGQGTNG FQLLRHAVKR
DLLPPRTPPY QGDVPPGIRN TICHMQQGIC RLFFCHSGTG QQHRQRCG*
mutated AA sequence MRQRLLPSVT SLLLVALLFP GSSQARHVNH SATEALGELR ERAPGQGTNG FQLLRHAVKR
DLLPPRTPPY QGDVPPGIRN TICRMQQGIC RLFFCHSGTG QQHRQRCG*
speed 2.51 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
back to results table
Yum, tasty mutations...

mutation t@sting

documentation

Prediction

polymorphism

Model: simple_aae, prob: 0.999999999999888 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr8:7308386T>CN/A show variant in all transcripts   IGV
HGNC symbol SPAG11B
Ensembl transcript ID ENST00000458665
Genbank transcript ID NM_058207
UniProt peptide Q08648
alteration type single base exchange
alteration region CDS
DNA changes c.92A>G
cDNA.144A>G
g.12811A>G
AA changes H31R Score: 29 explain score(s)
position(s) of altered AA
if AA alteration in CDS
31
frameshift no
known variant Reference ID: rs1042797
databasehomozygous (C/C)heterozygousallele carriers
1000G---
ExAC14826311517941
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-0.7340.005
-0.2930.01
(flanking)-0.1340.086
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc marginally increased12816wt: 0.2915 / mu: 0.2977 (marginal change - not scored)wt: GAAATACCATCTGCCATATGCAGCAAGGGATCTGCAGACTT
mu: GAAATACCATCTGCCGTATGCAGCAAGGGATCTGCAGACTT
 atgc|AGCA
distance from splice site 37
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      31DVPPGIRNTICHMQQGICRLFFCH
mutated  not conserved    31DVPPGIRNTICRMQQGICRLFFC
Ptroglodytes  not conserved  ENSPTRG00000019963  84DVPLGIRNTICRMQQGICRLFFC
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  not conserved  ENSMUSG00000059463  81PNYQIVNCKKSEGQCQEY-C
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
protein features no protein features affected
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 243 / 243
position (AA) of stopcodon in wt / mu AA sequence 81 / 81
position of stopcodon in wt / mu cDNA 295 / 295
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 53 / 53
chromosome 8
strand -1
last intron/exon boundary 108
theoretical NMD boundary in CDS 5
length of CDS 243
coding sequence (CDS) position 92
cDNA position
(for ins/del: last normal base / first normal base)
144
gDNA position
(for ins/del: last normal base / first normal base)
12811
chromosomal position
(for ins/del: last normal base / first normal base)
7308386
original gDNA sequence snippet AATTAGAAATACCATCTGCCATATGCAGCAAGGGATCTGCA
altered gDNA sequence snippet AATTAGAAATACCATCTGCCGTATGCAGCAAGGGATCTGCA
original cDNA sequence snippet AATTAGAAATACCATCTGCCATATGCAGCAAGGGATCTGCA
altered cDNA sequence snippet AATTAGAAATACCATCTGCCGTATGCAGCAAGGGATCTGCA
wildtype AA sequence MKVFFLFAVL FCLVQTNSGD VPPGIRNTIC HMQQGICRLF FCHSGEKKRD ICSDPWNRCC
VSNTDEEGKE KPEMDGRSGI *
mutated AA sequence MKVFFLFAVL FCLVQTNSGD VPPGIRNTIC RMQQGICRLF FCHSGEKKRD ICSDPWNRCC
VSNTDEEGKE KPEMDGRSGI *
speed 1.26 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
back to results table
Yum, tasty mutations...

mutation t@sting

documentation

Prediction

polymorphism

Model: without_aae, prob: 0.99999985147049 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • homozygous in TGP or ExAC
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr8:7308386T>CN/A show variant in all transcripts   IGV
HGNC symbol SPAG11B
Ensembl transcript ID ENST00000528168
Genbank transcript ID NM_058206
UniProt peptide N/A
alteration type single base exchange
alteration region 3'UTR
DNA changes cDNA.220A>G
g.12811A>G
AA changes N/A
position(s) of altered AA
if AA alteration in CDS
N/A
frameshift N/A
known variant Reference ID: rs1042797
databasehomozygous (C/C)heterozygousallele carriers
1000G---
ExAC14826311517941
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-0.7340.005
-0.2930.01
(flanking)-0.1340.086
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc marginally increased12816wt: 0.2915 / mu: 0.2977 (marginal change - not scored)wt: GAAATACCATCTGCCATATGCAGCAAGGGATCTGCAGACTT
mu: GAAATACCATCTGCCGTATGCAGCAAGGGATCTGCAGACTT
 atgc|AGCA
distance from splice site 37
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
N/A
protein features N/A
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 signal is predicted to be ok
conservation
nucleotide level for all changes - no scoring up to now
N/A
position of start ATG in wt / mu cDNA 53 / 53
chromosome 8
strand -1
last intron/exon boundary 184
theoretical NMD boundary in CDS 81
length of CDS 153
coding sequence (CDS) position N/A
cDNA position
(for ins/del: last normal base / first normal base)
220
gDNA position
(for ins/del: last normal base / first normal base)
12811
chromosomal position
(for ins/del: last normal base / first normal base)
7308386
original gDNA sequence snippet AATTAGAAATACCATCTGCCATATGCAGCAAGGGATCTGCA
altered gDNA sequence snippet AATTAGAAATACCATCTGCCGTATGCAGCAAGGGATCTGCA
original cDNA sequence snippet AATTAGAAATACCATCTGCCATATGCAGCAAGGGATCTGCA
altered cDNA sequence snippet AATTAGAAATACCATCTGCCGTATGCAGCAAGGGATCTGCA
wildtype AA sequence MKVFFLFAVL FCLVQTNSVH ISHREARGPS FRICVDFLGP RWARGCSTGN *
mutated AA sequence N/A
speed 1.10 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
back to results table
Yum, tasty mutations...

mutation t@sting

documentation

Prediction

polymorphism

Model: without_aae, prob: 0.99999985147049 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • homozygous in TGP or ExAC
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr8:7308386T>CN/A show variant in all transcripts   IGV
HGNC symbol SPAG11B
Ensembl transcript ID ENST00000361111
Genbank transcript ID NM_058202
UniProt peptide N/A
alteration type single base exchange
alteration region intron
DNA changes g.12811A>G
AA changes N/A
position(s) of altered AA
if AA alteration in CDS
N/A
frameshift N/A
known variant Reference ID: rs1042797
databasehomozygous (C/C)heterozygousallele carriers
1000G---
ExAC14826311517941
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-0.7340.005
-0.2930.01
(flanking)-0.1340.086
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc marginally increased12816wt: 0.2915 / mu: 0.2977 (marginal change - not scored)wt: GAAATACCATCTGCCATATGCAGCAAGGGATCTGCAGACTT
mu: GAAATACCATCTGCCGTATGCAGCAAGGGATCTGCAGACTT
 atgc|AGCA
distance from splice site 2815
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
N/A
protein features N/A
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 24 / 24
chromosome 8
strand -1
last intron/exon boundary 238
theoretical NMD boundary in CDS 164
length of CDS 249
coding sequence (CDS) position N/A
cDNA position
(for ins/del: last normal base / first normal base)
N/A
gDNA position
(for ins/del: last normal base / first normal base)
12811
chromosomal position
(for ins/del: last normal base / first normal base)
7308386
original gDNA sequence snippet AATTAGAAATACCATCTGCCATATGCAGCAAGGGATCTGCA
altered gDNA sequence snippet AATTAGAAATACCATCTGCCGTATGCAGCAAGGGATCTGCA
original cDNA sequence snippet N/A
altered cDNA sequence snippet N/A
wildtype AA sequence MRQRLLPSVT SLLLVALLFP GSSQARHVNH SATEALGELR ERAPGQGTNG FQLLRHAVKR
DLLPPRTPPY QGTGQQHRQR CG*
mutated AA sequence N/A
speed 1.32 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
back to results table
Yum, tasty mutations...

mutation t@sting

documentation

Prediction

polymorphism

Model: without_aae, prob: 0.99999985147049 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • homozygous in TGP or ExAC
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr8:7308386T>CN/A show variant in all transcripts   IGV
HGNC symbol SPAG11B
Ensembl transcript ID ENST00000297498
Genbank transcript ID NM_016512
UniProt peptide N/A
alteration type single base exchange
alteration region 3'UTR
DNA changes cDNA.494A>G
g.12811A>G
AA changes N/A
position(s) of altered AA
if AA alteration in CDS
N/A
frameshift N/A
known variant Reference ID: rs1042797
databasehomozygous (C/C)heterozygousallele carriers
1000G---
ExAC14826311517941
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-0.7340.005
-0.2930.01
(flanking)-0.1340.086
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc marginally increased12816wt: 0.2915 / mu: 0.2977 (marginal change - not scored)wt: GAAATACCATCTGCCATATGCAGCAAGGGATCTGCAGACTT
mu: GAAATACCATCTGCCGTATGCAGCAAGGGATCTGCAGACTT
 atgc|AGCA
distance from splice site 37
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
N/A
protein features N/A
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 signal is predicted to be ok
conservation
nucleotide level for all changes - no scoring up to now
N/A
position of start ATG in wt / mu cDNA 168 / 168
chromosome 8
strand -1
last intron/exon boundary 458
theoretical NMD boundary in CDS 240
length of CDS 312
coding sequence (CDS) position N/A
cDNA position
(for ins/del: last normal base / first normal base)
494
gDNA position
(for ins/del: last normal base / first normal base)
12811
chromosomal position
(for ins/del: last normal base / first normal base)
7308386
original gDNA sequence snippet AATTAGAAATACCATCTGCCATATGCAGCAAGGGATCTGCA
altered gDNA sequence snippet AATTAGAAATACCATCTGCCGTATGCAGCAAGGGATCTGCA
original cDNA sequence snippet AATTAGAAATACCATCTGCCATATGCAGCAAGGGATCTGCA
altered cDNA sequence snippet AATTAGAAATACCATCTGCCGTATGCAGCAAGGGATCTGCA
wildtype AA sequence MRQRLLPSVT SLLLVALLFP GSSQARHVNH SATEALGELR ERAPGQGTNG FQLLRHAVKR
DLLPPRTPPY QVHISHREAR GPSFRICVDF LGPRWARGCS TGN*
mutated AA sequence N/A
speed 1.36 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
back to results table

Problems