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QuickView for rs148080007;jsessionid=16FCC282A7DA52EC8703E2B06906C43D (snp)


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      • Human Human A|G
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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|G
Chromosomal Location:
chr 6 : 160080037 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
WTAP
Related URLs:
NCBI dbSNP


WTAP   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_004906
A56G NP_004897 Missense K19R
NM_152857
A56G NP_690596 Missense K19R
NM_152858
A56G NP_690597 Missense K19R