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QuickView for rs146247905;jsessionid=AE965446A2DABC210FCB1317C4ED3090 (snp)


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      • Human Human T|C
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Type:
SNP
Organism:
Homo sapiens
Alleles:
T|C
Chromosomal Location:
chr 13 : 27775364 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
FLT1
Related URLs:
NCBI dbSNP


FLT1   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_002019
G3957A NP_002010 Synonymous A1319A