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CTTTGAAACAGTGGGCTCTGTCTTA[C/G]TGGGGGCCAAAGTGAGCGAAACCAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 137570 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FLJ42351 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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FLJ42351 - uncharacterized LOC400999 | ||||||
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There are no transcripts associated with this gene. |
SLC20A1 - solute carrier family 20 member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005415.4 | 739 | Missense Mutation | CTG,GTG | L,V 77 | NP_005406.3 | |
XM_017004768.1 | 739 | UTR 5 | XP_016860257.1 | |||
XM_017004769.1 | 739 | UTR 5 | XP_016860258.1 | |||
XM_017004770.1 | 739 | UTR 5 | XP_016860259.1 | |||
XM_017004771.1 | 739 | UTR 5 | XP_016860260.1 |