Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCGTAGCGCTTGATGTACACTAAGT[C/T]GATAAAGTCTCGAGGGGAAATGGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607051 | ||||||||||||||||||||
Literature Links: |
STARD6 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 |
STARD6 - StAR related lipid transfer domain containing 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_139171.1 | 489 | Missense Mutation | AAC,GAC | N,D 113 | NP_631910.1 | |
XM_011525821.1 | 489 | Missense Mutation | AAC,GAC | N,D 113 | XP_011524123.1 | |
XM_017025552.1 | 489 | Missense Mutation | AAC,GAC | N,D 54 | XP_016881041.1 | |
XM_017025553.1 | 489 | Missense Mutation | AAC,GAC | N,D 54 | XP_016881042.1 | |
XM_017025554.1 | 489 | Missense Mutation | AAC,GAC | N,D 31 | XP_016881043.1 |