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Search Thermo Fisher Scientific
TGCAGTCCTTGCTGCGCCTGTCTTG[C/G]CAAAGCTATGGAGAGAAGTGAACAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609802 | ||||||||||||||||||||
Literature Links: |
MYEF2 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 |
MYEF2 - myelin expression factor 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001301210.1 | 2101 | Intron | NP_001288139.1 | |||
NM_016132.4 | 2101 | Intron | NP_057216.2 | |||
XM_005254422.4 | 2101 | Intron | XP_005254479.2 | |||
XM_005254424.4 | 2101 | Intron | XP_005254481.2 | |||
XM_005254425.4 | 2101 | UTR 3 | XP_005254482.2 | |||
XM_005254427.4 | 2101 | Intron | XP_005254484.1 | |||
XM_006720553.3 | 2101 | Intron | XP_006720616.1 | |||
XM_011521657.2 | 2101 | Intron | XP_011519959.1 | |||
XM_017022285.1 | 2101 | UTR 3 | XP_016877774.1 | |||
XM_017022286.1 | 2101 | UTR 3 | XP_016877775.1 | |||
XM_017022287.1 | 2101 | UTR 3 | XP_016877776.1 | |||
XM_017022288.1 | 2101 | Intron | XP_016877777.1 | |||
XM_017022289.1 | 2101 | Intron | XP_016877778.1 | |||
XM_017022290.1 | 2101 | Intron | XP_016877779.1 | |||
XM_017022291.1 | 2101 | UTR 3 | XP_016877780.1 | |||
XM_017022292.1 | 2101 | UTR 3 | XP_016877781.1 |
SLC24A5 - solute carrier family 24 member 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_205850.2 | 2101 | Missense Mutation | GCC,GGC | A,G 236 | NP_995322.1 | |
XM_017022079.1 | 2101 | Missense Mutation | GCC,GGC | A,G 154 | XP_016877568.1 | |
XM_017022080.1 | 2101 | Missense Mutation | GCC,GGC | A,G 154 | XP_016877569.1 |