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QuickView for rs142720998;jsessionid=9A8E0A19FCFEE142DEF245C05F598F03 (snp)


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Type:
SNP
Organism:
Homo sapiens
Alleles:
C|G
Chromosomal Location:
chr 19 : 12800692 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
RTBDN
Related URLs:
NCBI dbSNP


RTBDN   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_001080997
C245G NP_001074466 Missense P82R
NM_031429
C341G NP_113617 Missense P114R