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TTACTATTCCCATCACCACTAGAGT[G/T]TCGCTTGTTTAGAGACATTATGAAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600530 | ||||||||||||||||||||
Literature Links: |
MFSD9 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 |
MFSD9 - major facilitator superfamily domain containing 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001322080.1 | 1402 | Missense Mutation | AAC,CAC | N,H 401 | NP_001309009.1 | |
NM_001322081.1 | 1402 | Missense Mutation | AAC,CAC | N,H 401 | NP_001309010.1 | |
NM_032718.4 | 1402 | Missense Mutation | AAC,CAC | N,H 462 | NP_116107.3 | |
XM_011512005.2 | 1402 | Missense Mutation | AAC,CAC | N,H 401 | XP_011510307.1 | |
XM_011512006.2 | 1402 | Missense Mutation | AAC,CAC | N,H 337 | XP_011510308.1 | |
XM_011512007.2 | 1402 | Missense Mutation | AAC,CAC | N,H 321 | XP_011510309.1 |
SLC9A2 - solute carrier family 9 member A2 | ||||||
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There are no transcripts associated with this gene. |