Difference between revisions of "Sequence-based mutation analysis (Phenylketonuria)"

From Bioinformatikpedia
(Mutation dataset)
(Mutation dataset)
Line 50: Line 50:
 
| [http://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?rs=184148104 rs184148104] || <span style="background:#00FF00">C</span>AA⇒<span style="background:#00FF00">G</span>AA || 1123 || Gln(Q)-Glu(E) || 375 || ?
 
| [http://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?rs=184148104 rs184148104] || <span style="background:#00FF00">C</span>AA⇒<span style="background:#00FF00">G</span>AA || 1123 || Gln(Q)-Glu(E) || 375 || ?
 
|-
 
|-
  +
| [http://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?rs=199475695 rs180819807] || T<span style="background:#00FF00">T</span>T⇒T<span style="background:#00FF00">C</span>T || 1175 || Phe(F)-Ile(I) || 392 || ?
| x || x || x || x || x || x
 
 
|-
 
|-
 
| x || x || x || x || x || x
 
| x || x || x || x || x || x

Revision as of 18:27, 25 June 2013

Summary

...

Sequence-based mutation analysis

Mutation dataset

For the generation of the mutation dataset the following five SNPs from the HGMD database were used (25th June 2013): <figtable id="mutds_hgmd">

Missense mutations (SNPs) from HGMD
Accession Number Codon change Sequence position Amino acid change Codon number Disease Reference
CM000542 CAG⇒CTG 59 Gln(Q)-Leu(L) 20 Hyperphenylalaninaemia Hennermann (2000) Hum Mutat 15, 254
CM045080 GGT⇒AGT 307 Gly(G)-Ser(S) 103 Phenylketonuria Lee (2004) J Hum Genet 49, 617
CM910286 GCC⇒GTC 776 Ala(A)-Val(V) 259 Phenylketonuria Labrune (1991) Am J Hum Genet 48, 1115
CM010981 AAG⇒ACG 1022 Lys(K)-Thr(T) 341 Phenylketonuria Tyfield (1997) Am J Hum Genet 60, 388
CM090791 CCA⇒CAA 1247 Pro(P)-Gln(Q) 416 Hyperphenylalaninaemia Dobrowolski (2009) J Inherit Metab Dis 32, 10

</figtable>


Furthermore, the following five mutations from dbSNP were added (25th June 2013): <figtable id="mutds_dbSNP">

Missense mutations (SNPs) from dbSNP
Reference SNP Codon change Sequence position Amino acid change Codon number Disease
rs199475569 CAC⇒AAC 190 His(H)-Asn(N) 64 ?
rs62508752 ACA⇒CCA 796 Thr(T)-Ala(A) 266 Phenylketonuria
rs184148104 CAA⇒GAA 1123 Gln(Q)-Glu(E) 375 ?
rs180819807 TTT⇒TCT 1175 Phe(F)-Ile(I) 392 ?
x x x x x x

</figtable>

References

<references/>