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QuickView for rs140379038;jsessionid=2E2EDE944854D68EAC8414EC89E6AD75 (snp)


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      • Human Human A|C
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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|C
Chromosomal Location:
chr 9 : 70857990 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
FXN
Related URLs:
NCBI dbSNP


FXN   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_000144
C378A NP_000135 Synonymous S126S
NM_181425
C378A NP_852090 Synonymous S126S