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QuickView for rs144835873;jsessionid=71D26F062F9ED96292711CA98BD689B5 (snp)


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      • Human Human A|G
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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|G
Chromosomal Location:
chr 16 : 65444884 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
CA7
Related URLs:
NCBI dbSNP


CA7   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_001014435
G609A NP_001014435 Synonymous K203K
NM_005182
G777A NP_005173 Synonymous K259K