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QuickView for rs141764075;jsessionid=D84301CA5E64FA734FC7BD4A4EA5DABE (snp)


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      • Human Human A|G
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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|G
Chromosomal Location:
chr 19 : 53667452 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
CYTH2
Related URLs:
NCBI dbSNP


CYTH2   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_004228
G293A NP_004219 Missense R98H
NM_017457
G293A NP_059431 Missense R98H