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QuickView for rs140350379;jsessionid=A63607650046919EAA4BC83C67844B95 (snp)


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      • Human Human T|C
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Type:
SNP
Organism:
Homo sapiens
Alleles:
T|C
Chromosomal Location:
chr 13 : 35776580 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
SPART
Related URLs:
NCBI dbSNP


SPART   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_015087
A1923G NP_055902 Synonymous G641G