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QuickView for rs138122142;jsessionid=1B833FD65803A6FA0CED7572FB37A114 (snp)


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      • Human Human A|C
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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|C
Chromosomal Location:
chr 7 : 5717969 (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
G2010T NP_996994 Synonymous L670L
NM_207116
G1839T NP_996999 Synonymous L613L