Correlation Engine 2.0
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QuickView for rs61732497;jsessionid=77981DF9D22641FFA432C14931399C3B (snp)


    • Macaque Macaque A
      • Human Human C|T
      • Chimp Chimp G
    • Mouse Mouse A
    • Rat Rat A
Type:
snp
Organism:
Homo sapiens
Alleles:
C|T
Chromosomal Location:
chr 11 : 492115 (build 36.3)
Strand:
+
Flanking Sequence:
TCTAGCGTC [ C | T ] CTCAGCTCCTC
Update Date:
Apr 08 2008
Validated:
NO
Associated Gene(s):
LOC100128703RNH1
Related URLs:
NCBI dbSNP


LOC100128703   (intergenic)  QuickView

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

RNH1   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_002939
C48A NP_002930 Missense S16R
NM_203383
C48A NP_976317 Missense S16R
NM_203384
C48A NP_976318 Missense S16R
NM_203385
C48A NP_976319 Missense S16R
NM_203386
C48A NP_976320 Missense S16R
NM_203387
C48A NP_976321 Missense S16R
NM_203388
C48A NP_976322 Missense S16R
NM_203389
C48A NP_976323 Missense S16R
NM_002939
C48G NP_002930 Missense S16R
NM_203383
C48G NP_976317 Missense S16R
NM_203384
C48G NP_976318 Missense S16R
NM_203385
C48G NP_976319 Missense S16R
NM_203386
C48G NP_976320 Missense S16R
NM_203387
C48G NP_976321 Missense S16R
NM_203388
C48G NP_976322 Missense S16R
NM_203389
C48G NP_976323 Missense S16R