Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGTGAGGTGAGACTATCCAAAAACA[C/T]AGGAGGACAGTACTGCTTGAAACAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603567 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PIAS2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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PIAS2 - protein inhibitor of activated STAT 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001324046.1 | 2188 | Intron | NP_001310975.1 | |||
NM_001324047.1 | 2188 | Missense Mutation | ATG,GTG | M,V 559 | NP_001310976.1 | |
NM_001324048.1 | 2188 | Missense Mutation | ATG,GTG | M,V 558 | NP_001310977.1 | |
NM_001324049.1 | 2188 | Missense Mutation | ATG,GTG | M,V 558 | NP_001310978.1 | |
NM_001324051.1 | 2188 | Intron | NP_001310980.1 | |||
NM_001324052.1 | 2188 | Intron | NP_001310981.1 | |||
NM_001324053.1 | 2188 | Intron | NP_001310982.1 | |||
NM_001324054.1 | 2188 | Intron | NP_001310983.1 | |||
NM_001324055.1 | 2188 | Intron | NP_001310984.1 | |||
NM_001324057.1 | 2188 | Intron | NP_001310986.1 | |||
NM_001324058.1 | 2188 | Intron | NP_001310987.1 | |||
NM_001324059.1 | 2188 | Intron | NP_001310988.1 | |||
NM_001324060.1 | 2188 | Intron | NP_001310989.1 | |||
NM_004671.4 | 2188 | Missense Mutation | ATG,GTG | M,V 567 | NP_004662.2 | |
NM_173206.3 | 2188 | Intron | NP_775298.1 | |||
XM_005258377.3 | 2188 | Missense Mutation | ATG,GTG | M,V 572 | XP_005258434.1 | |
XM_005258379.3 | 2188 | Missense Mutation | ATG,GTG | M,V 568 | XP_005258436.1 | |
XM_006722571.3 | 2188 | Missense Mutation | ATG,GTG | M,V 607 | XP_006722634.1 | |
XM_006722572.3 | 2188 | Missense Mutation | ATG,GTG | M,V 606 | XP_006722635.1 | |
XM_006722573.2 | 2188 | Intron | XP_006722636.1 | |||
XM_011526258.2 | 2188 | Missense Mutation | ATG,GTG | M,V 566 | XP_011524560.1 | |
XM_011526259.2 | 2188 | Missense Mutation | ATG,GTG | M,V 559 | XP_011524561.1 | |
XM_017026068.1 | 2188 | Missense Mutation | ATG,GTG | M,V 559 | XP_016881557.1 | |
XM_017026069.1 | 2188 | Missense Mutation | ATG,GTG | M,V 558 | XP_016881558.1 | |
XM_017026070.1 | 2188 | Missense Mutation | ATG,GTG | M,V 558 | XP_016881559.1 | |
XM_017026071.1 | 2188 | Intron | XP_016881560.1 | |||
XM_017026072.1 | 2188 | Intron | XP_016881561.1 |