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QuickView for rs117875320;jsessionid=5C857CAECA219E62AE573C6C33EC51F8 (snp)


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      • Human Human T|G
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Type:
SNP
Organism:
Homo sapiens
Alleles:
T|G
Chromosomal Location:
chr 19 : 1209940 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
MIDN
Related URLs:
NCBI dbSNP


MIDN   (UTR)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_177401
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