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CCAGGCCGTCCAGAGGCGAGCGCTC[C/G]GGCGTGGGCAGCCCCAGGCCGTCGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 601618 MIM: 604784 | ||||||||||||||||||||
Literature Links: |
LINC00176 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 |
LINC00176 - long intergenic non-protein coding RNA 176 | ||||||
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There are no transcripts associated with this gene. |
SOX18 - SRY-box 18 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018419.2 | 755 | Silent Mutation | CCC,CCG | P,P 215 | NP_060889.1 |
TCEA2 - transcription elongation factor A2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003195.4 | 755 | Intron | NP_003186.1 | |||
NM_198723.1 | 755 | Intron | NP_942016.1 | |||
XM_005260229.3 | 755 | Intron | XP_005260286.1 | |||
XM_011529022.1 | 755 | Intron | XP_011527324.1 | |||
XM_011529023.1 | 755 | Intron | XP_011527325.1 | |||
XM_011529027.2 | 755 | Intron | XP_011527329.1 | |||
XM_017028036.1 | 755 | Intron | XP_016883525.1 | |||
XM_017028037.1 | 755 | Intron | XP_016883526.1 |