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QuickView for rs141859659 (snp)


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Type:
SNP
Organism:
Homo sapiens
Alleles:
T|C
Chromosomal Location:
chr 4 : 90968333 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
SNCA
Related URLs:
NCBI dbSNP, HapMap


SNCA   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_000345
G147A NP_000336 Synonymous V49V
NM_007308
G147A NP_009292 Synonymous V49V