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GGCCCTCCTAGCATACCTGCTGTTA[A/C]GGCTCATCTTCATTGATTTGCCTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601814 | ||||||||||||||||||||
Literature Links: |
FXYD2 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 |
FXYD2 - FXYD domain containing ion transport regulator 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001680.4 | 877 | Silent Mutation | NP_001671.2 | |||
NM_021603.3 | 877 | Silent Mutation | NP_067614.1 |
FXYD6-FXYD2 - FXYD6-FXYD2 readthrough | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001204268.1 | 877 | Silent Mutation | NP_001191197.1 | |||
NM_001243598.2 | 877 | UTR 3 | NP_001230527.1 |