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TCTGCATTTTTTAAACAAAGTATGT[A/G]CTGAGTCTGGATCTAATTGCAAACT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
GRAMD3 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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GRAMD3 - GRAM domain containing 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001146319.1 | Intron | NP_001139791.1 | ||||
NM_001146320.1 | Intron | NP_001139792.1 | ||||
NM_001146321.1 | Intron | NP_001139793.1 | ||||
NM_001146322.1 | Intron | NP_001139794.1 | ||||
NM_023927.2 | Intron | NP_076416.2 | ||||
XM_005272057.3 | Intron | XP_005272114.1 | ||||
XM_005272058.3 | Intron | XP_005272115.1 | ||||
XM_005272059.4 | Intron | XP_005272116.1 | ||||
XM_005272060.3 | Intron | XP_005272117.1 | ||||
XM_005272061.3 | Intron | XP_005272118.1 | ||||
XM_005272062.3 | Intron | XP_005272119.1 | ||||
XM_005272063.3 | Intron | XP_005272120.1 | ||||
XM_005272064.3 | Intron | XP_005272121.1 | ||||
XM_011543591.2 | Intron | XP_011541893.1 | ||||
XM_011543592.2 | Intron | XP_011541894.1 | ||||
XM_011543593.2 | Intron | XP_011541895.1 | ||||
XM_011543594.2 | Intron | XP_011541896.1 | ||||
XM_011543595.2 | Intron | XP_011541897.1 | ||||
XM_017009781.1 | Intron | XP_016865270.1 | ||||
XM_017009782.1 | Intron | XP_016865271.1 | ||||
XM_017009783.1 | Intron | XP_016865272.1 | ||||
XM_017009784.1 | Intron | XP_016865273.1 | ||||
XM_017009785.1 | Intron | XP_016865274.1 |
LOC105369178 - uncharacterized LOC105369178 | ||||||
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There are no transcripts associated with this gene. |