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: ENST00000388922
Querying Taster for transcript #2: ENST00000550683
Querying Taster for transcript #3: ENST00000419526
MT speed 0 s - this script 4.185667 s

Results

genesymbolpredictionprobabilitymodelprediction
problem		splicingClinVaramino acid changesvariant typedbSNP IDprotein lengthfile
ACVRL1disease_causing_automatic0.999999891114268simple_aaeaffected0R388Wsingle base exchangers28936401show file
ACVRL1disease_causing_automatic0.999999982133776simple_aaeaffected0R374Wsingle base exchangers28936401show file
ACVRL1disease_causing_automatic0.999999982133776simple_aaeaffected0R200Wsingle base exchangers28936401show file

Taster files

Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999999891114268 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CD050129)
  • known disease mutation at this position (HGMD CM970049)
  • known disease mutation: rs8249 (pathogenic)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr12:52309891C>TN/A show variant in all transcripts   IGV
HGNC symbol ACVRL1
Ensembl transcript ID ENST00000550683
Genbank transcript ID N/A
UniProt peptide P37023
alteration type single base exchange
alteration region CDS
DNA changes c.1162C>T
cDNA.1263C>T
g.9200C>T
AA changes R388W Score: 101 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 388
frameshift no
known variant Reference ID: rs28936401
Allele 'T' was neither found in ExAC nor 1000G.
known disease mutation: rs8249 (pathogenic for Telangiectasia, hereditary hemorrhagic, type 2|Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CD050129)

known disease mutation at this position, please check HGMD for details (HGMD ID CD050129)
known disease mutation at this position, please check HGMD for details (HGMD ID CM970049)

known disease mutation at this position, please check HGMD for details (HGMD ID CD050129)
known disease mutation at this position, please check HGMD for details (HGMD ID CM970049)
known disease mutation at this position, please check HGMD for details (HGMD ID CD050129)

known disease mutation at this position, please check HGMD for details (HGMD ID CD050129)
known disease mutation at this position, please check HGMD for details (HGMD ID CM970049)
known disease mutation at this position, please check HGMD for details (HGMD ID CD050129)
known disease mutation at this position, please check HGMD for details (HGMD ID CM970049)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)3.2191
0.8191
(flanking)5.8781
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Donor increased9193wt: 0.68 / mu: 0.96wt: GTGGGCACCAAGCGG
mu: GTGGGCACCAAGTGG		 GGGC|acca
distance from splice site 72
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      388DIGNNPRVGTKRYMAPEVLDEQIR
mutated  not conserved    388DIGNNPRVGTKWYMAPEVLDEQI
Ptroglodytes  all identical  ENSPTRG00000004963  374DIGNNPRVGTKRYMAPEVLDEQI
Mmulatta  all identical  ENSMMUG00000004982  381DIGNNPRVGTKRYMAPEVLDEQI
Fcatus  all identical  ENSFCAG00000000265  376DIGNNPRVGTKRYMAPEVLEEQI
Mmusculus  all identical  ENSMUSG00000000530  373DIGNNPRVGTKRYMAPEVLDEHI
Ggallus  no homologue    
Trubripes  all identical  ENSTRUG00000012725  341DVGNNPRVGTKRYMAPEVLDETI
Drerio  all identical  ENSDARG00000018179  369DVGTNPRVGTKRYMAPEVLDETI
Dmelanogaster  all identical  FBgn0003317  436DLGNNPKVGTKRYMAPEVLDESI
Celegans  no homologue    
Xtropicalis  all identical  ENSXETG00000031897  344DIGNNPRVGTKRYMAPEVLDETI
protein features
start (aa)end (aa)featuredetails 
142503TOPO_DOMCytoplasmic (Potential).lost
202492DOMAINProtein kinase.lost
390410HELIXmight get lost (downstream of altered splice site)
424428TURNmight get lost (downstream of altered splice site)
435442HELIXmight get lost (downstream of altered splice site)
455459STRANDmight get lost (downstream of altered splice site)
460462TURNmight get lost (downstream of altered splice site)
463469HELIXmight get lost (downstream of altered splice site)
476478HELIXmight get lost (downstream of altered splice site)
482491HELIXmight get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1554 / 1554
position (AA) of stopcodon in wt / mu AA sequence 518 / 518
position of stopcodon in wt / mu cDNA 1655 / 1655
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 102 / 102
chromosome 12
strand 1
last intron/exon boundary 1521
theoretical NMD boundary in CDS 1369
length of CDS 1554
coding sequence (CDS) position 1162
cDNA position
(for ins/del: last normal base / first normal base)		 1263
gDNA position
(for ins/del: last normal base / first normal base)		 9200
chromosomal position
(for ins/del: last normal base / first normal base)		 52309891
original gDNA sequence snippet ACCCGAGAGTGGGCACCAAGCGGTACATGGCACCCGAGGTG
altered gDNA sequence snippet ACCCGAGAGTGGGCACCAAGTGGTACATGGCACCCGAGGTG
original cDNA sequence snippet ACCCGAGAGTGGGCACCAAGCGGTACATGGCACCCGAGGTG
altered cDNA sequence snippet ACCCGAGAGTGGGCACCAAGTGGTACATGGCACCCGAGGTG
wildtype AA sequence MALTPPLLLL SAGTMTLGSP RKGLLMLLMA LVTQGDPVKP SRGPLVTCTC ESPHCKGPTC
RGAWCTVVLV REEGRHPQEH RGCGNLHREL CRGRPTEFVN HYCCDSHLCN HNVSLVLEAT
QPPSEQPGTD GQLALILGPV LALLALVALG VLGLWHVRRR QEKQRGLHSE LGESSLILKA
SEQGDSMLGD LLDSDCTTGS GSGLPFLVQR TVARQVALVE CVGKGRYGEV WRGLWHGESV
AVKIFSSRDE QSWFRETEIY NTVLLRHDNI LGFIASDMTS RNSSTQLWLI THYHEHGSLY
DFLQRQTLEP HLALRLAVSA ACGLAHLHVE IFGTQGKPAI AHRDFKSRNV LVKSNLQCCI
ADLGLAVMHS QGSDYLDIGN NPRVGTKRYM APEVLDEQIR TDCFESYKWT DIWAFGLVLW
EIARRTIVNG IVEDYRPPFY DVVPNDPSFE DMKKVVCVDQ QTPTIPNRLA ADPVLSGLAQ
MMRECWYPNP SARLTALRIK KTLQKISNSP EKPKVIQ*
mutated AA sequence MALTPPLLLL SAGTMTLGSP RKGLLMLLMA LVTQGDPVKP SRGPLVTCTC ESPHCKGPTC
RGAWCTVVLV REEGRHPQEH RGCGNLHREL CRGRPTEFVN HYCCDSHLCN HNVSLVLEAT
QPPSEQPGTD GQLALILGPV LALLALVALG VLGLWHVRRR QEKQRGLHSE LGESSLILKA
SEQGDSMLGD LLDSDCTTGS GSGLPFLVQR TVARQVALVE CVGKGRYGEV WRGLWHGESV
AVKIFSSRDE QSWFRETEIY NTVLLRHDNI LGFIASDMTS RNSSTQLWLI THYHEHGSLY
DFLQRQTLEP HLALRLAVSA ACGLAHLHVE IFGTQGKPAI AHRDFKSRNV LVKSNLQCCI
ADLGLAVMHS QGSDYLDIGN NPRVGTKWYM APEVLDEQIR TDCFESYKWT DIWAFGLVLW
EIARRTIVNG IVEDYRPPFY DVVPNDPSFE DMKKVVCVDQ QTPTIPNRLA ADPVLSGLAQ
MMRECWYPNP SARLTALRIK KTLQKISNSP EKPKVIQ*
speed 0.93 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

disease causing

 Model: simple_aae, prob: 0.999999982133776 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CD050129)
  • known disease mutation at this position (HGMD CM970049)
  • known disease mutation: rs8249 (pathogenic)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr12:52309891C>TN/A show variant in all transcripts   IGV
HGNC symbol ACVRL1
Ensembl transcript ID ENST00000388922
Genbank transcript ID NM_000020
UniProt peptide P37023
alteration type single base exchange
alteration region CDS
DNA changes c.1120C>T
cDNA.1403C>T
g.9200C>T
AA changes R374W Score: 101 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 374
frameshift no
known variant Reference ID: rs28936401
Allele 'T' was neither found in ExAC nor 1000G.
known disease mutation: rs8249 (pathogenic for Telangiectasia, hereditary hemorrhagic, type 2|Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CD050129)

known disease mutation at this position, please check HGMD for details (HGMD ID CD050129)
known disease mutation at this position, please check HGMD for details (HGMD ID CM970049)

known disease mutation at this position, please check HGMD for details (HGMD ID CD050129)
known disease mutation at this position, please check HGMD for details (HGMD ID CM970049)
known disease mutation at this position, please check HGMD for details (HGMD ID CD050129)

known disease mutation at this position, please check HGMD for details (HGMD ID CD050129)
known disease mutation at this position, please check HGMD for details (HGMD ID CM970049)
known disease mutation at this position, please check HGMD for details (HGMD ID CD050129)
known disease mutation at this position, please check HGMD for details (HGMD ID CM970049)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)3.2191
0.8191
(flanking)5.8781
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Donor increased9193wt: 0.68 / mu: 0.96wt: GTGGGCACCAAGCGG
mu: GTGGGCACCAAGTGG		 GGGC|acca
distance from splice site 72
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      374DIGNNPRVGTKRYMAPEVLDEQIR
mutated  not conserved    374DIGNNPRVGTKWYMAPEVLDEQI
Ptroglodytes  all identical  ENSPTRG00000004963  374DIGNNPRVGTKRYMAPEVLDEQI
Mmulatta  all identical  ENSMMUG00000004982  381DIGNNPRVGTKRYMAPEVLDEQI
Fcatus  all identical  ENSFCAG00000000265  376DIGNNPRVGTKRYMAPEVLEEQI
Mmusculus  all identical  ENSMUSG00000000530  373DIGNNPRVGTKRYMAPEVLDEHI
Ggallus  no homologue    
Trubripes  all identical  ENSTRUG00000012725  341DVGNNPRVGTKRYMAPEVLDETI
Drerio  all identical  ENSDARG00000018179  369DVGTNPRVGTKRYMAPEVLDETI
Dmelanogaster  all identical  FBgn0003317  436DLGNNPKVGTKRYMAPEVLDESI
Celegans  no homologue    
Xtropicalis  all identical  ENSXETG00000031897  344DIGNNPRVGTKRYMAPEVLDETI
protein features
start (aa)end (aa)featuredetails 
142503TOPO_DOMCytoplasmic (Potential).lost
202492DOMAINProtein kinase.lost
373375HELIXlost
378381HELIXmight get lost (downstream of altered splice site)
390410HELIXmight get lost (downstream of altered splice site)
424428TURNmight get lost (downstream of altered splice site)
435442HELIXmight get lost (downstream of altered splice site)
455459STRANDmight get lost (downstream of altered splice site)
460462TURNmight get lost (downstream of altered splice site)
463469HELIXmight get lost (downstream of altered splice site)
476478HELIXmight get lost (downstream of altered splice site)
482491HELIXmight get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1512 / 1512
position (AA) of stopcodon in wt / mu AA sequence 504 / 504
position of stopcodon in wt / mu cDNA 1795 / 1795
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 284 / 284
chromosome 12
strand 1
last intron/exon boundary 1661
theoretical NMD boundary in CDS 1327
length of CDS 1512
coding sequence (CDS) position 1120
cDNA position
(for ins/del: last normal base / first normal base)		 1403
gDNA position
(for ins/del: last normal base / first normal base)		 9200
chromosomal position
(for ins/del: last normal base / first normal base)		 52309891
original gDNA sequence snippet ACCCGAGAGTGGGCACCAAGCGGTACATGGCACCCGAGGTG
altered gDNA sequence snippet ACCCGAGAGTGGGCACCAAGTGGTACATGGCACCCGAGGTG
original cDNA sequence snippet ACCCGAGAGTGGGCACCAAGCGGTACATGGCACCCGAGGTG
altered cDNA sequence snippet ACCCGAGAGTGGGCACCAAGTGGTACATGGCACCCGAGGTG
wildtype AA sequence MTLGSPRKGL LMLLMALVTQ GDPVKPSRGP LVTCTCESPH CKGPTCRGAW CTVVLVREEG
RHPQEHRGCG NLHRELCRGR PTEFVNHYCC DSHLCNHNVS LVLEATQPPS EQPGTDGQLA
LILGPVLALL ALVALGVLGL WHVRRRQEKQ RGLHSELGES SLILKASEQG DSMLGDLLDS
DCTTGSGSGL PFLVQRTVAR QVALVECVGK GRYGEVWRGL WHGESVAVKI FSSRDEQSWF
RETEIYNTVL LRHDNILGFI ASDMTSRNSS TQLWLITHYH EHGSLYDFLQ RQTLEPHLAL
RLAVSAACGL AHLHVEIFGT QGKPAIAHRD FKSRNVLVKS NLQCCIADLG LAVMHSQGSD
YLDIGNNPRV GTKRYMAPEV LDEQIRTDCF ESYKWTDIWA FGLVLWEIAR RTIVNGIVED
YRPPFYDVVP NDPSFEDMKK VVCVDQQTPT IPNRLAADPV LSGLAQMMRE CWYPNPSARL
TALRIKKTLQ KISNSPEKPK VIQ*
mutated AA sequence MTLGSPRKGL LMLLMALVTQ GDPVKPSRGP LVTCTCESPH CKGPTCRGAW CTVVLVREEG
RHPQEHRGCG NLHRELCRGR PTEFVNHYCC DSHLCNHNVS LVLEATQPPS EQPGTDGQLA
LILGPVLALL ALVALGVLGL WHVRRRQEKQ RGLHSELGES SLILKASEQG DSMLGDLLDS
DCTTGSGSGL PFLVQRTVAR QVALVECVGK GRYGEVWRGL WHGESVAVKI FSSRDEQSWF
RETEIYNTVL LRHDNILGFI ASDMTSRNSS TQLWLITHYH EHGSLYDFLQ RQTLEPHLAL
RLAVSAACGL AHLHVEIFGT QGKPAIAHRD FKSRNVLVKS NLQCCIADLG LAVMHSQGSD
YLDIGNNPRV GTKWYMAPEV LDEQIRTDCF ESYKWTDIWA FGLVLWEIAR RTIVNGIVED
YRPPFYDVVP NDPSFEDMKK VVCVDQQTPT IPNRLAADPV LSGLAQMMRE CWYPNPSARL
TALRIKKTLQ KISNSPEKPK VIQ*
speed 0.48 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

disease causing

 Model: simple_aae, prob: 0.999999982133776 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CD050129)
  • known disease mutation at this position (HGMD CM970049)
  • known disease mutation: rs8249 (pathogenic)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr12:52309891C>TN/A show variant in all transcripts   IGV
HGNC symbol ACVRL1
Ensembl transcript ID ENST00000419526
Genbank transcript ID N/A
UniProt peptide P37023
alteration type single base exchange
alteration region CDS
DNA changes c.598C>T
cDNA.660C>T
g.9200C>T
AA changes R200W Score: 101 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 200
frameshift no
known variant Reference ID: rs28936401
Allele 'T' was neither found in ExAC nor 1000G.
known disease mutation: rs8249 (pathogenic for Telangiectasia, hereditary hemorrhagic, type 2|Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CD050129)

known disease mutation at this position, please check HGMD for details (HGMD ID CD050129)
known disease mutation at this position, please check HGMD for details (HGMD ID CM970049)

known disease mutation at this position, please check HGMD for details (HGMD ID CD050129)
known disease mutation at this position, please check HGMD for details (HGMD ID CM970049)
known disease mutation at this position, please check HGMD for details (HGMD ID CD050129)

known disease mutation at this position, please check HGMD for details (HGMD ID CD050129)
known disease mutation at this position, please check HGMD for details (HGMD ID CM970049)
known disease mutation at this position, please check HGMD for details (HGMD ID CD050129)
known disease mutation at this position, please check HGMD for details (HGMD ID CM970049)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)3.2191
0.8191
(flanking)5.8781
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Donor increased9193wt: 0.68 / mu: 0.96wt: GTGGGCACCAAGCGG
mu: GTGGGCACCAAGTGG		 GGGC|acca
distance from splice site 72
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      200DIGNNPRVGTKRYMAPEVLDEQIR
mutated  not conserved    200DIGNNPRVGTKWYMAPEVLDEQI
Ptroglodytes  all identical  ENSPTRG00000004963  374DIGNNPRVGTKRYMAPEVLDEQI
Mmulatta  all identical  ENSMMUG00000004982  381DIGNNPRVGTKRYMAPEVL
Fcatus  all identical  ENSFCAG00000000265  376DIGNNPRVGTKRYMAPEVLEEQI
Mmusculus  all identical  ENSMUSG00000000530  373DIGNNPRVGTKRYMAPEVLDEHI
Ggallus  no homologue    
Trubripes  all identical  ENSTRUG00000012725  341DVGNNPRVGTKRYMAPEVLDETI
Drerio  all identical  ENSDARG00000018179  369DVGTNPRVGTKRYMAPEVLDETI
Dmelanogaster  all identical  FBgn0003317  436DLGNNPKVGTKRYMAPEVLDESI
Celegans  no homologue    
Xtropicalis  all identical  ENSXETG00000031897  344DIGNNPRVGTKRYMAPEVLDETI
protein features
start (aa)end (aa)featuredetails 
142503TOPO_DOMCytoplasmic (Potential).lost
172201DOMAINGS.lost
198201HELIXlost
202492DOMAINProtein kinase.might get lost (downstream of altered splice site)
203211STRANDmight get lost (downstream of altered splice site)
208216NP_BINDATP (By similarity).might get lost (downstream of altered splice site)
214221STRANDmight get lost (downstream of altered splice site)
224231STRANDmight get lost (downstream of altered splice site)
229229BINDINGATP (By similarity).might get lost (downstream of altered splice site)
233235HELIXmight get lost (downstream of altered splice site)
236248HELIXmight get lost (downstream of altered splice site)
259265STRANDmight get lost (downstream of altered splice site)
272278STRANDmight get lost (downstream of altered splice site)
285291HELIXmight get lost (downstream of altered splice site)
296314HELIXmight get lost (downstream of altered splice site)
325327STRANDmight get lost (downstream of altered splice site)
330330ACT_SITEProton acceptor (By similarity).might get lost (downstream of altered splice site)
335338STRANDmight get lost (downstream of altered splice site)
344346STRANDmight get lost (downstream of altered splice site)
353355STRANDmight get lost (downstream of altered splice site)
357359STRANDmight get lost (downstream of altered splice site)
373375HELIXmight get lost (downstream of altered splice site)
378381HELIXmight get lost (downstream of altered splice site)
390410HELIXmight get lost (downstream of altered splice site)
424428TURNmight get lost (downstream of altered splice site)
435442HELIXmight get lost (downstream of altered splice site)
455459STRANDmight get lost (downstream of altered splice site)
460462TURNmight get lost (downstream of altered splice site)
463469HELIXmight get lost (downstream of altered splice site)
476478HELIXmight get lost (downstream of altered splice site)
482491HELIXmight get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 990 / 990
position (AA) of stopcodon in wt / mu AA sequence 330 / 330
position of stopcodon in wt / mu cDNA 1052 / 1052
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 63 / 63
chromosome 12
strand 1
last intron/exon boundary 918
theoretical NMD boundary in CDS 805
length of CDS 990
coding sequence (CDS) position 598
cDNA position
(for ins/del: last normal base / first normal base)		 660
gDNA position
(for ins/del: last normal base / first normal base)		 9200
chromosomal position
(for ins/del: last normal base / first normal base)		 52309891
original gDNA sequence snippet ACCCGAGAGTGGGCACCAAGCGGTACATGGCACCCGAGGTG
altered gDNA sequence snippet ACCCGAGAGTGGGCACCAAGTGGTACATGGCACCCGAGGTG
original cDNA sequence snippet ACCCGAGAGTGGGCACCAAGCGGTACATGGCACCCGAGGTG
altered cDNA sequence snippet ACCCGAGAGTGGGCACCAAGTGGTACATGGCACCCGAGGTG
wildtype AA sequence MALTPPLLLL SAGTMTLGSP RKGLLMLLMA LVTQGKGRYG EVWRGLWHGE SVAVKIFSSR
DEQSWFRETE IYNTVLLRHD NILGFIASDM TSRNSSTQLW LITHYHEHGS LYDFLQRQTL
EPHLALRLAV SAACGLAHLH VEIFGTQGKP AIAHRDFKSR NVLVKSNLQC CIADLGLAVM
HSQGSDYLDI GNNPRVGTKR YMAPEVLDEQ IRTDCFESYK WTDIWAFGLV LWEIARRTIV
NGIVEDYRPP FYDVVPNDPS FEDMKKVVCV DQQTPTIPNR LAADPVLSGL AQMMRECWYP
NPSARLTALR IKKTLQKISN SPEKPKVIQ*
mutated AA sequence MALTPPLLLL SAGTMTLGSP RKGLLMLLMA LVTQGKGRYG EVWRGLWHGE SVAVKIFSSR
DEQSWFRETE IYNTVLLRHD NILGFIASDM TSRNSSTQLW LITHYHEHGS LYDFLQRQTL
EPHLALRLAV SAACGLAHLH VEIFGTQGKP AIAHRDFKSR NVLVKSNLQC CIADLGLAVM
HSQGSDYLDI GNNPRVGTKW YMAPEVLDEQ IRTDCFESYK WTDIWAFGLV LWEIARRTIV
NGIVEDYRPP FYDVVPNDPS FEDMKKVVCV DQQTPTIPNR LAADPVLSGL AQMMRECWYP
NPSARLTALR IKKTLQKISN SPEKPKVIQ*
speed 1.18 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