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QuickView for rs146356109;jsessionid=1B833FD65803A6FA0CED7572FB37A114 (snp)


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      • Human Human T|C
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Type:
SNP
Organism:
Homo sapiens
Alleles:
T|C
Chromosomal Location:
chr 7 : 5629308 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
RNF216
Related URLs:
NCBI dbSNP


RNF216   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_207111
G2481A NP_996994 Synonymous P827P
NM_207116
G2310A NP_996999 Synonymous P770P