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QuickView for rs119475043;jsessionid=A04B429338F79DFFD01DF058D0C05103 (snp)


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      • Human Human A|C
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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|C
Chromosomal Location:
chr 19 : 59318993 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
PRPF31
Related URLs:
NCBI dbSNP


PRPF31   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_015629
C581A NP_056444 Missense A194E