Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTTGCTGGGTCTGCCCACAGCTGTG[A/G]TCTATGGCTCCCTGGCTCTCTTCAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
MFSD13A 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 |
MFSD13A - major facilitator superfamily domain containing 13A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024789.3 | 894 | Missense Mutation | ATC,GTC | I,V 18 | NP_079065.2 | |
XM_006717973.3 | 894 | Missense Mutation | ATC,GTC | I,V 18 | XP_006718036.1 | |
XM_006717974.3 | 894 | Missense Mutation | ATC,GTC | I,V 18 | XP_006718037.1 | |
XM_011540160.2 | 894 | Missense Mutation | ATC,GTC | I,V 18 | XP_011538462.1 | |
XM_011540163.2 | 894 | Missense Mutation | ATC,GTC | I,V 18 | XP_011538465.1 | |
XM_011540167.2 | 894 | Missense Mutation | ATC,GTC | I,V 18 | XP_011538469.1 | |
XM_011540169.2 | 894 | Missense Mutation | ATC,GTC | I,V 18 | XP_011538471.1 | |
XM_017016654.1 | 894 | Missense Mutation | ATC,GTC | I,V 18 | XP_016872143.1 | |
XM_017016655.1 | 894 | Missense Mutation | ATC,GTC | I,V 18 | XP_016872144.1 | |
XM_017016656.1 | 894 | Missense Mutation | ATC,GTC | I,V 18 | XP_016872145.1 | |
XM_017016657.1 | 894 | Missense Mutation | ATC,GTC | I,V 18 | XP_016872146.1 | |
XM_017016658.1 | 894 | Missense Mutation | ATC,GTC | I,V 18 | XP_016872147.1 | |
XM_017016659.1 | 894 | Missense Mutation | ATC,GTC | I,V 18 | XP_016872148.1 | |
XM_017016660.1 | 894 | Intron | XP_016872149.1 | |||
XM_017016661.1 | 894 | Missense Mutation | ATC,GTC | I,V 18 | XP_016872150.1 | |
XM_017016662.1 | 894 | Missense Mutation | ATC,GTC | I,V 18 | XP_016872151.1 |