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TCTTTTAACTCAGCCTCTCAACCTA[C/T]CAGAATAATGAAGTTATGCTGTGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
12 submissions
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Phenotype: |
MIM: 608172 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DHDDS PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
DHDDS - dehydrodolichyl diphosphate synthase subunit | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001243564.1 | Intron | NP_001230493.1 | ||||
NM_001243565.1 | Intron | NP_001230494.1 | ||||
NM_001319959.1 | Intron | NP_001306888.1 | ||||
NM_024887.3 | Intron | NP_079163.2 | ||||
NM_205861.2 | Intron | NP_995583.1 | ||||
XM_006710912.2 | Intron | XP_006710975.1 | ||||
XM_006710913.2 | Intron | XP_006710976.1 | ||||
XM_006710914.2 | Intron | XP_006710977.1 | ||||
XM_006710915.2 | Intron | XP_006710978.1 | ||||
XM_006710916.2 | Intron | XP_006710979.1 | ||||
XM_006710917.2 | Intron | XP_006710980.1 | ||||
XM_006710918.2 | Intron | XP_006710981.1 | ||||
XM_011542183.2 | Intron | XP_011540485.1 | ||||
XM_011542184.2 | Intron | XP_011540486.1 | ||||
XM_011542185.2 | Intron | XP_011540487.1 | ||||
XM_011542186.2 | Intron | XP_011540488.1 | ||||
XM_017002379.1 | Intron | XP_016857868.1 | ||||
XM_017002380.1 | Intron | XP_016857869.1 | ||||
XM_017002381.1 | Intron | XP_016857870.1 | ||||
XM_017002382.1 | Intron | XP_016857871.1 | ||||
XM_017002383.1 | Intron | XP_016857872.1 | ||||
XM_017002384.1 | Intron | XP_016857873.1 |