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QuickView for rs146262464;jsessionid=B374E96E27D4FA5871188558B2941FAD (snp)


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Type:
SNP
Organism:
Homo sapiens
Alleles:
T|C
Chromosomal Location:
chr 14 : 104759141 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
BRF1
Related URLs:
NCBI dbSNP


BRF1   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_001519
G1204A NP_001510 Missense G402S
NM_145685
G592A NP_663718 Missense G198S