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QuickView for rs141604707;jsessionid=592680166CD503E14F04BC04F3A90AB6 (snp)


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      • Human Human T|C
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Type:
SNP
Organism:
Homo sapiens
Alleles:
T|C
Chromosomal Location:
chr 18 : 75312707 (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
C1806T NP_006153 Synonymous S602S
NM_172387
C1767T NP_765975 Synonymous S589S
NM_172388
C390T NP_765976 Synonymous S130S
NM_172389
C1767T NP_765977 Synonymous S589S
NM_172390
C1806T NP_765978 Synonymous S602S