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QuickView for rs147948047;jsessionid=ED0090D57616933F9C138A6E04CC95BB (snp)


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      • Human Human T|C
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Type:
SNP
Organism:
Homo sapiens
Alleles:
T|C
Chromosomal Location:
chr 14 : 80732308 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
GTF2A1
Related URLs:
NCBI dbSNP


GTF2A1   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_015859
A509G NP_056943 Missense N170S
NM_201595
A392G NP_963889 Missense N131S