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 3 transcript(s)...
Querying Taster for transcript #1: ENST00000301093
Querying Taster for transcript #2: ENST00000540331
Querying Taster for transcript #3: ENST00000391785
MT speed 0 s - this script 3.925663 s

Results


genesymbolpredictionprobabilitymodelprediction
problem
splicingClinVaramino acid changesvariant typedbSNP IDprotein lengthfile
ZNF701polymorphism_automatic1.36589628496608e-11simple_aaeaffectedD9Ysingle base exchangers8104138show file
ZNF701polymorphism_automatic1.36589628496608e-11simple_aaeaffectedD9Ysingle base exchangers8104138show file
ZNF701polymorphism_automatic1.08548094956973e-07without_aaeaffectedsingle base exchangers8104138show file

Taster files

Yum, tasty mutations...

mutation t@sting

documentation

Prediction

polymorphism

Model: simple_aae, prob: 0.999999999986341 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
  • protein features (might be) affected
  • splice site changes
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr19:53075519G>TN/A show variant in all transcripts   IGV
HGNC symbol ZNF701
Ensembl transcript ID ENST00000301093
Genbank transcript ID N/A
UniProt peptide Q9NV72
alteration type single base exchange
alteration region CDS
DNA changes c.25G>T
cDNA.60G>T
g.1994G>T
AA changes D9Y Score: 160 explain score(s)
position(s) of altered AA
if AA alteration in CDS
9
frameshift no
known variant Reference ID: rs8104138
databasehomozygous (T/T)heterozygousallele carriers
1000G31511161431
ExAC97723033280
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H3K9me3, Histone, Histone 3 Lysine 9 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.210.018
0.210.016
(flanking)-1.1270.013
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased1992wt: 0.41 / mu: 0.63wt: GGGGTTTCTCCATGTTGGTCAGGATGGTCTCGAACTCCCGA
mu: GGGGTTTCTCCATGTTGGTCAGTATGGTCTCGAACTCCCGA
 gtca|GGAT
Donor increased1992wt: 0.77 / mu: 0.87wt: TGGTCAGGATGGTCT
mu: TGGTCAGTATGGTCT
 GTCA|ggat
Donor gained19870.74mu: CATGTTGGTCAGTAT TGTT|ggtc
distance from splice site 30
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      9 MGFLHVGQDGLELPTSGDPPA
mutated  not conserved    9 MGFLHVGQYGLELPTSGDPPAS
Ptroglodytes  no homologue    
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
protein features
start (aa)end (aa)featuredetails 
880DOMAINKRAB.lost
270292ZN_FINGC2H2-type 1.might get lost (downstream of altered splice site)
298320ZN_FINGC2H2-type 2.might get lost (downstream of altered splice site)
326348ZN_FINGC2H2-type 3.might get lost (downstream of altered splice site)
354376ZN_FINGC2H2-type 4.might get lost (downstream of altered splice site)
382404ZN_FINGC2H2-type 5.might get lost (downstream of altered splice site)
410432ZN_FINGC2H2-type 6.might get lost (downstream of altered splice site)
438460ZN_FINGC2H2-type 7.might get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1596 / 1596
position (AA) of stopcodon in wt / mu AA sequence 532 / 532
position of stopcodon in wt / mu cDNA 1631 / 1631
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 36 / 36
chromosome 19
strand 1
last intron/exon boundary 376
theoretical NMD boundary in CDS 290
length of CDS 1596
coding sequence (CDS) position 25
cDNA position
(for ins/del: last normal base / first normal base)
60
gDNA position
(for ins/del: last normal base / first normal base)
1994
chromosomal position
(for ins/del: last normal base / first normal base)
53075519
original gDNA sequence snippet GGTTTCTCCATGTTGGTCAGGATGGTCTCGAACTCCCGACA
altered gDNA sequence snippet GGTTTCTCCATGTTGGTCAGTATGGTCTCGAACTCCCGACA
original cDNA sequence snippet GGTTTCTCCATGTTGGTCAGGATGGTCTCGAACTCCCGACA
altered cDNA sequence snippet GGTTTCTCCATGTTGGTCAGTATGGTCTCGAACTCCCGACA
wildtype AA sequence MGFLHVGQDG LELPTSGDPP ASASQSAGIT GVSHRTQPPC FEGLTSKDLV REEKTRKRKR
KAKESGMALL QGLLTFRDVA IEFSQEEWKC LDPAQRTLYR DVMLENYRNL VSLDTSSKCM
MKMFSSTGQG NTEVVHTGTL QIHASHHIGD TCFQEIEKDI HDFVFQWQEN ETNGHEALMT
KTKKLMSSTE RHDQRHAGNK PIKNELGSSF HSHLPEVHIF HPEGKIGNQV EKAINDAFSV
SASQRISCRP KTRISNKYRN NFLQSSLLTQ KREVHTREKS FQRNESGKAF NGSSLLKKHQ
IIHLGDKQYK CDVCGKDFHQ KRYLACHRCH TGENPYTCNE CGKTFSHNSA LLVHKAIHTG
EKPYKCNECG KVFNQQSNLA RHHRVHTGEK PYKCEECDKV FSRKSHLERH RRIHTGEKPY
KCKVCDKAFR RDSHLAQHTV IHTGEKPYKC NECGKTFVQN SSLVMHKVIH TGEKRYKCNE
CGKVFNHKSN LACHRRLHTG EKPYKCNECG KVFNRKSNLE RHHRLHTGKK S*
mutated AA sequence MGFLHVGQYG LELPTSGDPP ASASQSAGIT GVSHRTQPPC FEGLTSKDLV REEKTRKRKR
KAKESGMALL QGLLTFRDVA IEFSQEEWKC LDPAQRTLYR DVMLENYRNL VSLDTSSKCM
MKMFSSTGQG NTEVVHTGTL QIHASHHIGD TCFQEIEKDI HDFVFQWQEN ETNGHEALMT
KTKKLMSSTE RHDQRHAGNK PIKNELGSSF HSHLPEVHIF HPEGKIGNQV EKAINDAFSV
SASQRISCRP KTRISNKYRN NFLQSSLLTQ KREVHTREKS FQRNESGKAF NGSSLLKKHQ
IIHLGDKQYK CDVCGKDFHQ KRYLACHRCH TGENPYTCNE CGKTFSHNSA LLVHKAIHTG
EKPYKCNECG KVFNQQSNLA RHHRVHTGEK PYKCEECDKV FSRKSHLERH RRIHTGEKPY
KCKVCDKAFR RDSHLAQHTV IHTGEKPYKC NECGKTFVQN SSLVMHKVIH TGEKRYKCNE
CGKVFNHKSN LACHRRLHTG EKPYKCNECG KVFNRKSNLE RHHRLHTGKK S*
speed 0.92 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: 0.999999999986341 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
  • protein features (might be) affected
  • splice site changes
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr19:53075519G>TN/A show variant in all transcripts   IGV
HGNC symbol ZNF701
Ensembl transcript ID ENST00000540331
Genbank transcript ID NM_001172655
UniProt peptide Q9NV72
alteration type single base exchange
alteration region CDS
DNA changes c.25G>T
cDNA.250G>T
g.1994G>T
AA changes D9Y Score: 160 explain score(s)
position(s) of altered AA
if AA alteration in CDS
9
frameshift no
known variant Reference ID: rs8104138
databasehomozygous (T/T)heterozygousallele carriers
1000G31511161431
ExAC97723033280
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H3K9me3, Histone, Histone 3 Lysine 9 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.210.018
0.210.016
(flanking)-1.1270.013
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased1992wt: 0.41 / mu: 0.63wt: GGGGTTTCTCCATGTTGGTCAGGATGGTCTCGAACTCCCGA
mu: GGGGTTTCTCCATGTTGGTCAGTATGGTCTCGAACTCCCGA
 gtca|GGAT
Donor increased1992wt: 0.77 / mu: 0.87wt: TGGTCAGGATGGTCT
mu: TGGTCAGTATGGTCT
 GTCA|ggat
Donor gained19870.74mu: CATGTTGGTCAGTAT TGTT|ggtc
distance from splice site 27
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      9 MGFLHVGQDGLELPTSGDPPA
mutated  not conserved    9 MGFLHVGQYGLELPTSGDPPAS
Ptroglodytes  no homologue    
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
protein features
start (aa)end (aa)featuredetails 
880DOMAINKRAB.lost
270292ZN_FINGC2H2-type 1.might get lost (downstream of altered splice site)
298320ZN_FINGC2H2-type 2.might get lost (downstream of altered splice site)
326348ZN_FINGC2H2-type 3.might get lost (downstream of altered splice site)
354376ZN_FINGC2H2-type 4.might get lost (downstream of altered splice site)
382404ZN_FINGC2H2-type 5.might get lost (downstream of altered splice site)
410432ZN_FINGC2H2-type 6.might get lost (downstream of altered splice site)
438460ZN_FINGC2H2-type 7.might get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1596 / 1596
position (AA) of stopcodon in wt / mu AA sequence 532 / 532
position of stopcodon in wt / mu cDNA 1821 / 1821
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 226 / 226
chromosome 19
strand 1
last intron/exon boundary 566
theoretical NMD boundary in CDS 290
length of CDS 1596
coding sequence (CDS) position 25
cDNA position
(for ins/del: last normal base / first normal base)
250
gDNA position
(for ins/del: last normal base / first normal base)
1994
chromosomal position
(for ins/del: last normal base / first normal base)
53075519
original gDNA sequence snippet GGTTTCTCCATGTTGGTCAGGATGGTCTCGAACTCCCGACA
altered gDNA sequence snippet GGTTTCTCCATGTTGGTCAGTATGGTCTCGAACTCCCGACA
original cDNA sequence snippet GGTTTCTCCATGTTGGTCAGGATGGTCTCGAACTCCCGACA
altered cDNA sequence snippet GGTTTCTCCATGTTGGTCAGTATGGTCTCGAACTCCCGACA
wildtype AA sequence MGFLHVGQDG LELPTSGDPP ASASQSAGIT GVSHRTQPPC FEGLTSKDLV REEKTRKRKR
KAKESGMALL QGLLTFRDVA IEFSQEEWKC LDPAQRTLYR DVMLENYRNL VSLDTSSKCM
MKMFSSTGQG NTEVVHTGTL QIHASHHIGD TCFQEIEKDI HDFVFQWQEN ETNGHEALMT
KTKKLMSSTE RHDQRHAGNK PIKNELGSSF HSHLPEVHIF HPEGKIGNQV EKAINDAFSV
SASQRISCRP KTRISNKYRN NFLQSSLLTQ KREVHTREKS FQRNESGKAF NGSSLLKKHQ
IIHLGDKQYK CDVCGKDFHQ KRYLACHRCH TGENPYTCNE CGKTFSHNSA LLVHKAIHTG
EKPYKCNECG KVFNQQSNLA RHHRVHTGEK PYKCEECDKV FSRKSHLERH RRIHTGEKPY
KCKVCDKAFR RDSHLAQHTV IHTGEKPYKC NECGKTFVQN SSLVMHKVIH TGEKRYKCNE
CGKVFNHKSN LACHRRLHTG EKPYKCNECG KVFNRKSNLE RHHRLHTGKK S*
mutated AA sequence MGFLHVGQYG LELPTSGDPP ASASQSAGIT GVSHRTQPPC FEGLTSKDLV REEKTRKRKR
KAKESGMALL QGLLTFRDVA IEFSQEEWKC LDPAQRTLYR DVMLENYRNL VSLDTSSKCM
MKMFSSTGQG NTEVVHTGTL QIHASHHIGD TCFQEIEKDI HDFVFQWQEN ETNGHEALMT
KTKKLMSSTE RHDQRHAGNK PIKNELGSSF HSHLPEVHIF HPEGKIGNQV EKAINDAFSV
SASQRISCRP KTRISNKYRN NFLQSSLLTQ KREVHTREKS FQRNESGKAF NGSSLLKKHQ
IIHLGDKQYK CDVCGKDFHQ KRYLACHRCH TGENPYTCNE CGKTFSHNSA LLVHKAIHTG
EKPYKCNECG KVFNQQSNLA RHHRVHTGEK PYKCEECDKV FSRKSHLERH RRIHTGEKPY
KCKVCDKAFR RDSHLAQHTV IHTGEKPYKC NECGKTFVQN SSLVMHKVIH TGEKRYKCNE
CGKVFNHKSN LACHRRLHTG EKPYKCNECG KVFNRKSNLE RHHRLHTGKK S*
speed 0.55 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: 0.999999891451905 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • homozygous in TGP or ExAC
  • protein features (might be) affected
  • splice site changes
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr19:53075519G>TN/A show variant in all transcripts   IGV
HGNC symbol ZNF701
Ensembl transcript ID ENST00000391785
Genbank transcript ID NM_018260
UniProt peptide Q9NV72
alteration type single base exchange
alteration region intron
DNA changes g.1994G>T
AA changes N/A
position(s) of altered AA
if AA alteration in CDS
N/A
frameshift N/A
known variant Reference ID: rs8104138
databasehomozygous (T/T)heterozygousallele carriers
1000G31511161431
ExAC97723033280
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H3K9me3, Histone, Histone 3 Lysine 9 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.210.018
0.210.016
(flanking)-1.1270.013
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites splice site change before start ATG (at aa -23) |
effectgDNA positionscoredetection sequence  exon-intron border
Acc increased1992wt: 0.41 / mu: 0.63wt: GGGGTTTCTCCATGTTGGTCAGGATGGTCTCGAACTCCCGA
mu: GGGGTTTCTCCATGTTGGTCAGTATGGTCTCGAACTCCCGA
 gtca|GGAT
Donor increased1992wt: 0.77 / mu: 0.87wt: TGGTCAGGATGGTCT
mu: TGGTCAGTATGGTCT
 GTCA|ggat
Donor gained19870.74mu: CATGTTGGTCAGTAT TGTT|ggtc
distance from splice site 1811
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
N/A
protein features
start (aa)end (aa)featuredetails 
880DOMAINKRAB.might get lost (downstream of altered splice site)
270292ZN_FINGC2H2-type 1.might get lost (downstream of altered splice site)
298320ZN_FINGC2H2-type 2.might get lost (downstream of altered splice site)
326348ZN_FINGC2H2-type 3.might get lost (downstream of altered splice site)
354376ZN_FINGC2H2-type 4.might get lost (downstream of altered splice site)
382404ZN_FINGC2H2-type 5.might get lost (downstream of altered splice site)
410432ZN_FINGC2H2-type 6.might get lost (downstream of altered splice site)
438460ZN_FINGC2H2-type 7.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 130 / 130
chromosome 19
strand 1
last intron/exon boundary 272
theoretical NMD boundary in CDS 92
length of CDS 1398
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)
1994
chromosomal position
(for ins/del: last normal base / first normal base)
53075519
original gDNA sequence snippet GGTTTCTCCATGTTGGTCAGGATGGTCTCGAACTCCCGACA
altered gDNA sequence snippet GGTTTCTCCATGTTGGTCAGTATGGTCTCGAACTCCCGACA
original cDNA sequence snippet N/A
altered cDNA sequence snippet N/A
wildtype AA sequence MALLQGLLTF RDVAIEFSQE EWKCLDPAQR TLYRDVMLEN YRNLVSLDTS SKCMMKMFSS
TGQGNTEVVH TGTLQIHASH HIGDTCFQEI EKDIHDFVFQ WQENETNGHE ALMTKTKKLM
SSTERHDQRH AGNKPIKNEL GSSFHSHLPE VHIFHPEGKI GNQVEKAIND AFSVSASQRI
SCRPKTRISN KYRNNFLQSS LLTQKREVHT REKSFQRNES GKAFNGSSLL KKHQIIHLGD
KQYKCDVCGK DFHQKRYLAC HRCHTGENPY TCNECGKTFS HNSALLVHKA IHTGEKPYKC
NECGKVFNQQ SNLARHHRVH TGEKPYKCEE CDKVFSRKSH LERHRRIHTG EKPYKCKVCD
KAFRRDSHLA QHTVIHTGEK PYKCNECGKT FVQNSSLVMH KVIHTGEKRY KCNECGKVFN
HKSNLACHRR LHTGEKPYKC NECGKVFNRK SNLERHHRLH TGKKS*
mutated AA sequence N/A
speed 0.73 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