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TAGCATTGCTGTTAGTGTGCCACTT[C/T]CACCAACCAAGAGCCACCAAAGGGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 611759 | ||||||||||||||||||||
Literature Links: |
STARD3NL 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 |
STARD3NL - STARD3 N-terminal like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032016.3 | Intron | NP_114405.1 | ||||
XM_005249880.1 | Intron | XP_005249937.1 | ||||
XM_005249881.2 | Intron | XP_005249938.1 | ||||
XM_011515572.1 | Intron | XP_011513874.1 | ||||
XM_017012692.1 | Intron | XP_016868181.1 | ||||
XM_017012693.1 | Intron | XP_016868182.1 | ||||
XM_017012694.1 | Intron | XP_016868183.1 | ||||
XM_017012695.1 | Intron | XP_016868184.1 | ||||
XM_017012696.1 | Intron | XP_016868185.1 | ||||
XM_017012697.1 | Intron | XP_016868186.1 | ||||
XM_017012698.1 | Intron | XP_016868187.1 |