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CCCCAGCCTCTTTTCATACCAAATA[C/T]TGAGCCGGGTTATCTTTCTAAAGCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612086 MIM: 601697 | ||||||||||||||||||||
Literature Links: |
HMSD 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 |
HMSD - histocompatibility minor serpin domain containing | ||||||
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There are no transcripts associated with this gene. |
SERPINB8 - serpin family B member 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001031848.1 | Intron | NP_001027018.1 | ||||
NM_001276490.1 | Intron | NP_001263419.1 | ||||
NM_002640.3 | Intron | NP_002631.3 | ||||
NM_198833.1 | Intron | NP_942130.1 | ||||
XM_006722484.2 | Intron | XP_006722547.1 | ||||
XM_011526025.1 | Intron | XP_011524327.1 | ||||
XM_017025790.1 | Intron | XP_016881279.1 | ||||
XM_017025791.1 | Intron | XP_016881280.1 | ||||
XM_017025792.1 | Intron | XP_016881281.1 |