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QuickView for rs142608987;jsessionid=80D825B9FD3C126FCCF4A9BA5EA50439 (snp)


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      • Human Human C|G
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Type:
SNP
Organism:
Homo sapiens
Alleles:
C|G
Chromosomal Location:
chr 14 : 66717289 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
GPHN
Related URLs:
NCBI dbSNP


GPHN   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_001024218
G2093C NP_001019389 Missense S698T
NM_020806
G2192C NP_065857 Missense S731T