Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTGCCCTTGCCCTTGCCCCCATTCC[A/G]GGACCTGGTTACACCCTTGCCTCCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300363 | ||||||||||||||||||||
Literature Links: |
ARMCX2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
ARMCX2 - armadillo repeat containing, X-linked 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282231.1 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | NP_001269160.1 | |
NM_014782.6 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | NP_055597.1 | |
NM_177949.3 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | NP_808818.1 | |
XM_005278109.1 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | XP_005278166.1 | |
XM_005278110.1 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | XP_005278167.1 | |
XM_005278111.1 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | XP_005278168.1 | |
XM_005278113.1 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | XP_005278170.1 | |
XM_005278114.1 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | XP_005278171.1 | |
XM_005278115.1 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | XP_005278172.1 | |
XM_005278116.1 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | XP_005278173.1 | |
XM_005278117.1 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | XP_005278174.1 | |
XM_011531071.1 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | XP_011529373.1 | |
XM_011531072.1 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | XP_011529374.1 | |
XM_017029987.1 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | XP_016885476.1 | |
XM_017029988.1 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | XP_016885477.1 | |
XM_017029989.1 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | XP_016885478.1 | |
XM_017029990.1 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | XP_016885479.1 | |
XM_017029991.1 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | XP_016885480.1 | |
XM_017029992.1 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | XP_016885481.1 | |
XM_017029993.1 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | XP_016885482.1 | |
XM_017029994.1 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | XP_016885483.1 | |
XM_017029995.1 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | XP_016885484.1 | |
XM_017029996.1 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | XP_016885485.1 | |
XM_017029997.1 | 1451 | Missense Mutation | CGG,TGG | R,W 290 | XP_016885486.1 |