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QuickView for rs145940146;jsessionid=9FFAE934FB3087E69516070C64E2A936 (snp)


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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|G
Chromosomal Location:
chr 20 : 49566831 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
NFATC2
Related URLs:
NCBI dbSNP


NFATC2   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_012340
C1231T NP_036472 Missense R411W
NM_173091
C1231T NP_775114 Missense R411W