Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999999999979106 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM020708)
  • known disease mutation: rs16248 (pathogenic)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr2:49190705C>TN/A show variant in all transcripts   IGV
HGNC symbol FSHR
Ensembl transcript ID ENST00000541117
Genbank transcript ID N/A
UniProt peptide P23945
alteration type single base exchange
alteration region CDS
DNA changes c.463G>A
cDNA.1016G>A
g.190972G>A
AA changes A155T Score: 58 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 155
frameshift no
known variant Reference ID: rs121909661
databasehomozygous (T/T)heterozygousallele carriers
1000G---
ExAC011

known disease mutation: rs16248 (pathogenic for Ovarian dysgenesis 1) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM020708)

known disease mutation at this position, please check HGMD for details (HGMD ID CM020708)
known disease mutation at this position, please check HGMD for details (HGMD ID CM020708)
regulatory features N/A
phyloP / phastCons
PhyloPPhastCons
(flanking)5.8771
5.8771
(flanking)-0.2970.95
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 increased190973wt: 0.8661 / mu: 0.8682 (marginal change - not scored)wt: AATCTACCTGCTGCTCATTGCATCAGTTGATATCCATACCA
mu: AATCTACCTGCTGCTCATTACATCAGTTGATATCCATACCA		 ttgc|ATCA
Acc marginally increased190977wt: 0.9373 / mu: 0.9378 (marginal change - not scored)wt: TACCTGCTGCTCATTGCATCAGTTGATATCCATACCAAGAG
mu: TACCTGCTGCTCATTACATCAGTTGATATCCATACCAAGAG		 atca|GTTG
Acc increased190975wt: 0.33 / mu: 0.59wt: TCTACCTGCTGCTCATTGCATCAGTTGATATCCATACCAAG
mu: TCTACCTGCTGCTCATTACATCAGTTGATATCCATACCAAG		 gcat|CAGT
Donor marginally increased190977wt: 0.6551 / mu: 0.7065 (marginal change - not scored)wt: GCATCAGTTGATATC
mu: ACATCAGTTGATATC		 ATCA|gttg
distance from splice site 401
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      155DLCIGIYLLLIASVDIHTKSQYHN
mutated  not conserved    155DLCIGIYLLLITSVDIHTKSQYH
Ptroglodytes  all identical  ENSPTRG00000011914  419DLCIGIYLLLIASVDIHTKSQYH
Mmulatta  all identical  ENSMMUG00000017196  419DLCIGIYLLLIASVDIHTKSQYH
Fcatus  all identical  ENSFCAG00000001215  419DLCIGIYLLLIASVDIYTKSQYH
Mmusculus  all identical  ENSMUSG00000032937  418DLCIGIYLLLIASVDIHTKSQYH
Ggallus  all identical  ENSGALG00000009100  419DLCIGIYLLFIASVDIQTKSRYY
Trubripes  no homologue    
Drerio  all identical  ENSDARG00000071494  400DLCMGIYLLLIAAVDIHTQSRYY
Dmelanogaster  all identical  FBgn0016650  546DLCLGLYLLLVACIDAHSMGEYF
Celegans  all identical  C50H2.1  487TGIYLAVLAIADAKMSDEYY
Xtropicalis  all identical  ENSXETG00000025827  321DLCMGVYLLLIAAVDIKTKSQYY
protein features
start (aa)end (aa)featuredetails 
18366TOPO_DOMExtracellular (Potential).lost
144169REPEATLRR 5.lost
168171STRANDmight get lost (downstream of altered splice site)
170192REPEATLRR 6.might get lost (downstream of altered splice site)
173176STRANDmight get lost (downstream of altered splice site)
187192TURNmight get lost (downstream of altered splice site)
191191CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
193199STRANDmight get lost (downstream of altered splice site)
193216REPEATLRR 7.might get lost (downstream of altered splice site)
197198CONFLICTEL -> AV (in Ref. 1; AAA52477).might get lost (downstream of altered splice site)
199199CARBOHYDN-linked (GlcNAc...) (Potential).might get lost (downstream of altered splice site)
211216TURNmight get lost (downstream of altered splice site)
217240REPEATLRR 8.might get lost (downstream of altered splice site)
221224STRANDmight get lost (downstream of altered splice site)
235237STRANDmight get lost (downstream of altered splice site)
241259REPEATLRR 9.might get lost (downstream of altered splice site)
243245STRANDmight get lost (downstream of altered splice site)
258260TURNmight get lost (downstream of altered splice site)
266268STRANDmight get lost (downstream of altered splice site)
272280HELIXmight get lost (downstream of altered splice site)
293293CARBOHYDN-linked (GlcNAc...) (By similarity).might get lost (downstream of altered splice site)
295295CONFLICTS -> P (in Ref. 8; CAA48179).might get lost (downstream of altered splice site)
318318CARBOHYDN-linked (GlcNAc...) (Potential).might get lost (downstream of altered splice site)
345348STRANDmight get lost (downstream of altered splice site)
367387TRANSMEMHelical; Name=1; (Potential).might get lost (downstream of altered splice site)
388398TOPO_DOMCytoplasmic (Potential).might get lost (downstream of altered splice site)
399421TRANSMEMHelical; Name=2; (Potential).might get lost (downstream of altered splice site)
422443TOPO_DOMExtracellular (Potential).might get lost (downstream of altered splice site)
442442DISULFIDBy similarity.might get lost (downstream of altered splice site)
444465TRANSMEMHelical; Name=3; (Potential).might get lost (downstream of altered splice site)
466485TOPO_DOMCytoplasmic (Potential).might get lost (downstream of altered splice site)
486508TRANSMEMHelical; Name=4; (Potential).might get lost (downstream of altered splice site)
509528TOPO_DOMExtracellular (Potential).might get lost (downstream of altered splice site)
517517DISULFIDBy similarity.might get lost (downstream of altered splice site)
529550TRANSMEMHelical; Name=5; (Potential).might get lost (downstream of altered splice site)
551573TOPO_DOMCytoplasmic (Potential).might get lost (downstream of altered splice site)
574597TRANSMEMHelical; Name=6; (Potential).might get lost (downstream of altered splice site)
598608TOPO_DOMExtracellular (Potential).might get lost (downstream of altered splice site)
609630TRANSMEMHelical; Name=7; (Potential).might get lost (downstream of altered splice site)
631695TOPO_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 1296 / 1296
position (AA) of stopcodon in wt / mu AA sequence 432 / 432
position of stopcodon in wt / mu cDNA 1849 / 1849
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 554 / 554
chromosome 2
strand -1
last intron/exon boundary 616
theoretical NMD boundary in CDS 12
length of CDS 1296
coding sequence (CDS) position 463
cDNA position
(for ins/del: last normal base / first normal base)		 1016
gDNA position
(for ins/del: last normal base / first normal base)		 190972
chromosomal position
(for ins/del: last normal base / first normal base)		 49190705
original gDNA sequence snippet GAATCTACCTGCTGCTCATTGCATCAGTTGATATCCATACC
altered gDNA sequence snippet GAATCTACCTGCTGCTCATTACATCAGTTGATATCCATACC
original cDNA sequence snippet GAATCTACCTGCTGCTCATTGCATCAGTTGATATCCATACC
altered cDNA sequence snippet GAATCTACCTGCTGCTCATTACATCAGTTGATATCCATACC
wildtype AA sequence MEASLTYPSH CCAFANWRRQ ISELHPICNK SILRQEVDYM TQARGQRSSL AEDNESSYSR
GFDMTYTEFD YDLCNEVVDV TCSPKPDAFN PCEDIMGYNI LRVLIWFISI LAITGNIIVL
VILTTSQYKL TVPRFLMCNL AFADLCIGIY LLLIASVDIH TKSQYHNYAI DWQTGAGCDA
AGFFTVFASE LSVYTLTAIT LERWHTITHA MQLDCKVQLR HAASVMVMGW IFAFAAALFP
IFGISSYMKV SICLPMDIDS PLSQLYVMSL LVLNVLAFVV ICGCYIHIYL TVRNPNIVSS
SSDTRIAKRM AMLIFTDFLC MAPISFFAIS ASLKVPLITV SKAKILLVLF HPINSCANPF
LYAIFTKNFR RDFFILLSKC GCYEMQAQIY RTETSSTVHN THPRNGHCSS APRVTSGSTY
ILVPLSHLAQ N*
mutated AA sequence MEASLTYPSH CCAFANWRRQ ISELHPICNK SILRQEVDYM TQARGQRSSL AEDNESSYSR
GFDMTYTEFD YDLCNEVVDV TCSPKPDAFN PCEDIMGYNI LRVLIWFISI LAITGNIIVL
VILTTSQYKL TVPRFLMCNL AFADLCIGIY LLLITSVDIH TKSQYHNYAI DWQTGAGCDA
AGFFTVFASE LSVYTLTAIT LERWHTITHA MQLDCKVQLR HAASVMVMGW IFAFAAALFP
IFGISSYMKV SICLPMDIDS PLSQLYVMSL LVLNVLAFVV ICGCYIHIYL TVRNPNIVSS
SSDTRIAKRM AMLIFTDFLC MAPISFFAIS ASLKVPLITV SKAKILLVLF HPINSCANPF
LYAIFTKNFR RDFFILLSKC GCYEMQAQIY RTETSSTVHN THPRNGHCSS APRVTSGSTY
ILVPLSHLAQ N*
speed 0.96 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