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QuickView for rs116094927;jsessionid=F31F086E4750819C1153368337BEEED9 (snp)


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      • Human Human T|C
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Type:
SNP
Organism:
Homo sapiens
Alleles:
T|C
Chromosomal Location:
chr 3 : 132182157 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
ATP2C1
Related URLs:
NCBI dbSNP


ATP2C1   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_001001485
T1783C NP_001001485 Missense S595P
NM_001001486
T1783C NP_001001486 Missense S595P
NM_001001487
T1783C NP_001001487 Missense S595P
NM_014382
T1783C NP_055197 Missense S595P