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QuickView for rs145064111;jsessionid=49EC1279D8155C14D93FCE70FCE23998 (snp)


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Type:
SNP
Organism:
Homo sapiens
Alleles:
T|C
Chromosomal Location:
chr 11 : 10779115 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
EIF4G2
Related URLs:
NCBI dbSNP


EIF4G2   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_001042559
A1395G NP_001036024 Synonymous P465P
NM_001418
A1509G NP_001409 Synonymous P503P