Yum, tasty mutations...

mutation t@sting

documentation

Prediction

polymorphism

Model: simple_aae, prob: 0.999972920871891 (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) chr6:46827073A>GN/A show variant in all transcripts   IGV
HGNC symbol ADGRF5
Ensembl transcript ID ENST00000283296
Genbank transcript ID NM_001098518
UniProt peptide Q8IZF2
alteration type single base exchange
alteration region CDS
DNA changes c.2567T>C
cDNA.2856T>C
g.95608T>C
AA changes M856T Score: 81 explain score(s)
position(s) of altered AA
if AA alteration in CDS
856
frameshift no
known variant Reference ID: rs547499
databasehomozygous (G/G)heterozygousallele carriers
1000G7799981777
ExAC26418-200696349
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-0.5030.001
0.9230.276
(flanking)0.6680.396
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Donor marginally increased95612wt: 0.9673 / mu: 0.9937 (marginal change - not scored)wt: ATGGTAATCAAGTCC
mu: ACGGTAATCAAGTCC
 GGTA|atca
Donor increased95608wt: 0.85 / mu: 0.94wt: CAGCATGGTAATCAA
mu: CAGCACGGTAATCAA
 GCAT|ggta
Donor increased95599wt: 0.45 / mu: 0.58wt: GCAGATGAGCAGCAT
mu: GCAGATGAGCAGCAC
 AGAT|gagc
distance from splice site 188
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      856SFSQTNVQMSSMVIKSSHPETYQQ
mutated  not conserved    856SFSQTNVQMSSTVIKSSHPETYQ
Ptroglodytes  all identical  ENSPTRG00000018240  856SFSQTNVQMSSMVIKSSHPKTYQ
Mmulatta  all identical  ENSMMUG00000023002  852SFFRTNVQMSSMVIKSSHPKTYQ
Fcatus  no homologue    
Mmusculus  all identical  ENSMUSG00000056492  855FLAHPNVQMKSMVIKRGHPQIYQ
Ggallus  all identical  ENSGALG00000016718  798HLSTETLELQGMVVTEHSHADYN
Trubripes  not conserved  ENSTRUG00000017329  1199EIVTERIKLN----KTSFDTS
Drerio  no homologue    
Dmelanogaster  no alignment  FBgn0039818  n/a
Celegans  no homologue    
Xtropicalis  no homologue    
protein features
start (aa)end (aa)featuredetails 
221006TOPO_DOMExtracellular (Potential).lost
931931CARBOHYDN-linked (GlcNAc...) (Potential).might get lost (downstream of altered splice site)
9511002DOMAINGPS.might get lost (downstream of altered splice site)
963963CARBOHYDN-linked (GlcNAc...) (Potential).might get lost (downstream of altered splice site)
982982CARBOHYDN-linked (GlcNAc...) (Potential).might get lost (downstream of altered splice site)
990991SITECleavage (By similarity).might get lost (downstream of altered splice site)
10071027TRANSMEMHelical; Name=1; (Potential).might get lost (downstream of altered splice site)
10281053TOPO_DOMCytoplasmic (Potential).might get lost (downstream of altered splice site)
10541074TRANSMEMHelical; Name=2; (Potential).might get lost (downstream of altered splice site)
10751075CONFLICTQ -> R (in Ref. 5; AL832125).might get lost (downstream of altered splice site)
10751090TOPO_DOMExtracellular (Potential).might get lost (downstream of altered splice site)
10911111TRANSMEMHelical; Name=3; (Potential).might get lost (downstream of altered splice site)
11121128TOPO_DOMCytoplasmic (Potential).might get lost (downstream of altered splice site)
11291149TRANSMEMHelical; Name=4; (Potential).might get lost (downstream of altered splice site)
11501173TOPO_DOMExtracellular (Potential).might get lost (downstream of altered splice site)
11741194TRANSMEMHelical; Name=5; (Potential).might get lost (downstream of altered splice site)
11951220TOPO_DOMCytoplasmic (Potential).might get lost (downstream of altered splice site)
12211241TRANSMEMHelical; Name=6; (Potential).might get lost (downstream of altered splice site)
12421244TOPO_DOMExtracellular (Potential).might get lost (downstream of altered splice site)
12451265TRANSMEMHelical; Name=7; (Potential).might get lost (downstream of altered splice site)
12661346TOPO_DOMCytoplasmic (Potential).might get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 4041 / 4041
position (AA) of stopcodon in wt / mu AA sequence 1347 / 1347
position of stopcodon in wt / mu cDNA 4330 / 4330
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 290 / 290
chromosome 6
strand -1
last intron/exon boundary 4251
theoretical NMD boundary in CDS 3911
length of CDS 4041
coding sequence (CDS) position 2567
cDNA position
(for ins/del: last normal base / first normal base)
2856
gDNA position
(for ins/del: last normal base / first normal base)
95608
chromosomal position
(for ins/del: last normal base / first normal base)
46827073
original gDNA sequence snippet TAATGTGCAGATGAGCAGCATGGTAATCAAGTCCAGCCACC
altered gDNA sequence snippet TAATGTGCAGATGAGCAGCACGGTAATCAAGTCCAGCCACC
original cDNA sequence snippet TAATGTGCAGATGAGCAGCATGGTAATCAAGTCCAGCCACC
altered cDNA sequence snippet TAATGTGCAGATGAGCAGCACGGTAATCAAGTCCAGCCACC
wildtype AA sequence MKSPRRTTLC LMFIVIYSSK AALNWNYEST IHPLSLHEHE PAGEEALRQK RAVATKSPTA
EEYTVNIEIS FENASFLDPI KAYLNSLSFP IHGNNTDQIT DILSINVTTV CRPAGNEIWC
SCETGYGWPR ERCLHNLICQ ERDVFLPGHH CSCLKELPPN GPFCLLQEDV TLNMRVRLNV
GFQEDLMNTS SALYRSYKTD LETAFRKGYG ILPGFKGVTV TGFKSGSVVV TYEVKTTPPS
LELIHKANEQ VVQSLNQTYK MDYNSFQAVT INESNFFVTP EIIFEGDTVS LVCEKEVLSS
NVSWRYEEQQ LEIQNSSRFS IYTALFNNMT SVSKLTIHNI TPGDAGEYVC KLILDIFEYE
CKKKIDVMPI QILANEEMKV MCDNNPVSLN CCSQGNVNWS KVEWKQEGKI NIPGTPETDI
DSSCSRYTLK ADGTQCPSGS SGTTVIYTCE FISAYGARGS ANIKVTFISV ANLTITPDPI
SVSEGQNFSI KCISDVSNYD EVYWNTSAGI KIYQRFYTTR RYLDGAESVL TVKTSTREWN
GTYHCIFRYK NSYSIATKDV IVHPLPLKLN IMVDPLEATV SCSGSHHIKC CIEEDGDYKV
TFHTGSSSLP AAKEVNKKQV CYKHNFNASS VSWCSKTVDV CCHFTNAANN SVWSPSMKLN
LVPGENITCQ DPVIGVGEPG KVIQKLCRFS NVPSSPESPI GGTITYKCVG SQWEEKRNDC
ISAPINSLLQ MAKALIKSPS QDEMLPTYLK DLSISIDKAE HEISSSPGSL GAIINILDLL
STVPTQVNSE MMTHVLSTVN VILGKPVLNT WKVLQQQWTN QSSQLLHSVE RFSQALQSGD
SPPLSFSQTN VQMSSMVIKS SHPETYQQRF VFPYFDLWGN VVIDKSYLEN LQSDSSIVTM
AFPTLQAILA QDIQENNFAE SLVMTTTVSH NTTMPFRISM TFKNNSPSGG ETKCVFWNFR
LANNTGGWDS SGCYVEEGDG DNVTCICDHL TSFSILMSPD SPDPSSLLGI LLDIISYVGV
GFSILSLAAC LVVEAVVWKS VTKNRTSYMR HTCIVNIAAS LLVANTWFIV VAAIQDNRYI
LCKTACVAAT FFIHFFYLSV FFWMLTLGLM LFYRLVFILH ETSRSTQKAI AFCLGYGCPL
AISVITLGAT QPREVYTRKN VCWLNWEDTK ALLAFAIPAL IIVVVNITIT IVVITKILRP
SIGDKPCKQE KSSLFQISKS IGVLTPLLGL TWGFGLTTVF PGTNLVFHII FAILNVFQGL
FILLFGCLWD LKVQEALLNK FSLSRWSSQH SKSTSLGSST PVFSMSSPIS RRFNNLFGKT
GTYNVSTPEA TSSSLENSSS ASSLLN*
mutated AA sequence MKSPRRTTLC LMFIVIYSSK AALNWNYEST IHPLSLHEHE PAGEEALRQK RAVATKSPTA
EEYTVNIEIS FENASFLDPI KAYLNSLSFP IHGNNTDQIT DILSINVTTV CRPAGNEIWC
SCETGYGWPR ERCLHNLICQ ERDVFLPGHH CSCLKELPPN GPFCLLQEDV TLNMRVRLNV
GFQEDLMNTS SALYRSYKTD LETAFRKGYG ILPGFKGVTV TGFKSGSVVV TYEVKTTPPS
LELIHKANEQ VVQSLNQTYK MDYNSFQAVT INESNFFVTP EIIFEGDTVS LVCEKEVLSS
NVSWRYEEQQ LEIQNSSRFS IYTALFNNMT SVSKLTIHNI TPGDAGEYVC KLILDIFEYE
CKKKIDVMPI QILANEEMKV MCDNNPVSLN CCSQGNVNWS KVEWKQEGKI NIPGTPETDI
DSSCSRYTLK ADGTQCPSGS SGTTVIYTCE FISAYGARGS ANIKVTFISV ANLTITPDPI
SVSEGQNFSI KCISDVSNYD EVYWNTSAGI KIYQRFYTTR RYLDGAESVL TVKTSTREWN
GTYHCIFRYK NSYSIATKDV IVHPLPLKLN IMVDPLEATV SCSGSHHIKC CIEEDGDYKV
TFHTGSSSLP AAKEVNKKQV CYKHNFNASS VSWCSKTVDV CCHFTNAANN SVWSPSMKLN
LVPGENITCQ DPVIGVGEPG KVIQKLCRFS NVPSSPESPI GGTITYKCVG SQWEEKRNDC
ISAPINSLLQ MAKALIKSPS QDEMLPTYLK DLSISIDKAE HEISSSPGSL GAIINILDLL
STVPTQVNSE MMTHVLSTVN VILGKPVLNT WKVLQQQWTN QSSQLLHSVE RFSQALQSGD
SPPLSFSQTN VQMSSTVIKS SHPETYQQRF VFPYFDLWGN VVIDKSYLEN LQSDSSIVTM
AFPTLQAILA QDIQENNFAE SLVMTTTVSH NTTMPFRISM TFKNNSPSGG ETKCVFWNFR
LANNTGGWDS SGCYVEEGDG DNVTCICDHL TSFSILMSPD SPDPSSLLGI LLDIISYVGV
GFSILSLAAC LVVEAVVWKS VTKNRTSYMR HTCIVNIAAS LLVANTWFIV VAAIQDNRYI
LCKTACVAAT FFIHFFYLSV FFWMLTLGLM LFYRLVFILH ETSRSTQKAI AFCLGYGCPL
AISVITLGAT QPREVYTRKN VCWLNWEDTK ALLAFAIPAL IIVVVNITIT IVVITKILRP
SIGDKPCKQE KSSLFQISKS IGVLTPLLGL TWGFGLTTVF PGTNLVFHII FAILNVFQGL
FILLFGCLWD LKVQEALLNK FSLSRWSSQH SKSTSLGSST PVFSMSSPIS RRFNNLFGKT
GTYNVSTPEA TSSSLENSSS ASSLLN*
speed 0.63 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