Correlation Engine 2.0
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QuickView for rs1064180;jsessionid=D0C52CE705AF9B8BBF7E596A712AACBF (snp)


    • Macaque Macaque C
      • Human Human C|T
      • Chimp Chimp C
    • Mouse Mouse C
    • Rat Rat C
Type:
snp
Organism:
Homo sapiens
Alleles:
C|T
Chromosomal Location:
chr 11 : 118470898 (build 36.3)
Strand:
-
Flanking Sequence:
CACCCAGGC [ C | T ] TCCCAGGAGTA
Update Date:
Oct 04 2004
Validated:
NO
Associated Gene(s):
HMBSH2AFXDPAGT1
Related URLs:
NCBI dbSNP


HMBS   (intergenic)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
-
- - - -

H2AFX   (promoter / exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_002105
C417T NP_002096 Synonymous A139A

DPAGT1   (intergenic)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
-
- - - -