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TTCCATTCACACTCCCATCTCTGGG[C/T]GTCCTCAAGATAACCCGATGTTCCC
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614551 | |||||||||||||||||||||||
Literature Links: |
SERINC5 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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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 |
SERINC5 - serine incorporator 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001174071.2 | Intron | NP_001167542.1 | ||||
NM_001174072.2 | Intron | NP_001167543.1 | ||||
NM_178276.6 | Intron | NP_840060.1 | ||||
XM_011543304.1 | Intron | XP_011541606.1 | ||||
XM_017009323.1 | Intron | XP_016864812.1 | ||||
XM_017009324.1 | Intron | XP_016864813.1 | ||||
XM_017009325.1 | Intron | XP_016864814.1 | ||||
XM_017009326.1 | Intron | XP_016864815.1 |
Set Membership: |
HapMap |