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QuickView for rs138150995;jsessionid=592680166CD503E14F04BC04F3A90AB6 (snp)


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      • Human Human A|G
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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|G
Chromosomal Location:
chr 18 : 75294615 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
NFATC1
Related URLs:
NCBI dbSNP


NFATC1   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_006162
G1275A NP_006153 Synonymous P425P
NM_172387
G1236A NP_765975 Synonymous P412P
NM_172389
G1236A NP_765977 Synonymous P412P
NM_172390
G1275A NP_765978 Synonymous P425P