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CTTGTTCCTGCTGGGTATCCTCATC[A/G]TCATCAGTAAGTGCGACCCATTCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602359 MIM: 606669 MIM: 606684 | ||||||||||||||||||||
Literature Links: |
FXYD1 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 |
FXYD1 - FXYD domain containing ion transport regulator 1 | ||||||
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There are no transcripts associated with this gene. |
FXYD5 - FXYD domain containing ion transport regulator 5 | ||||||
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There are no transcripts associated with this gene. |
FXYD7 - FXYD domain containing ion transport regulator 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022006.1 | 214 | Missense Mutation | ATC,GTC | I,V 44 | NP_071289.1 |