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QuickView for rs114705520;jsessionid=0A414EBB90C7336CEA90DCF8A71698FD (snp)


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      • Human Human T|C
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Type:
SNP
Organism:
Homo sapiens
Alleles:
T|C
Chromosomal Location:
chr 1 : 114749710 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
TRIM33
Related URLs:
NCBI dbSNP


TRIM33   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_015906
G2613A NP_056990 Synonymous S871S
NM_033020
G2613A NP_148980 Synonymous S871S