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GTCCCACAGATGTCGCCCTCTGGTC[A/G]CCTGTGTCTTCTCACCATCGTTGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606669 MIM: 606684 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FXYD5 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
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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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FXYD5 - FXYD domain containing ion transport regulator 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001164605.1 | 105 | Missense Mutation | CAC,CGC | H,R 6 | NP_001158077.1 | |
NM_001320912.1 | 105 | Missense Mutation | CAC,CGC | H,R 6 | NP_001307841.1 | |
NM_001320913.1 | 105 | Missense Mutation | CAC,CGC | H,R 6 | NP_001307842.1 | |
NM_014164.5 | 105 | Missense Mutation | CAC,CGC | H,R 6 | NP_054883.3 | |
NM_144779.2 | 105 | Missense Mutation | CAC,CGC | H,R 6 | NP_659003.1 |
FXYD7 - FXYD domain containing ion transport regulator 7 | ||||||
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There are no transcripts associated with this gene. |