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NHSL1
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
NHSL1 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | ||||||
|---|---|---|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba)
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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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| NHSL1 - NHS like 1 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001144060.1 | Intron | NP_001137532.1 | ||||
| NM_020464.1 | Intron | NP_065197.1 | ||||
| XM_005267062.4 | Intron | XP_005267119.1 | ||||
| XM_011535965.2 | Intron | XP_011534267.1 | ||||
| XM_011535966.2 | Intron | XP_011534268.1 | ||||
| XM_011535967.2 | Intron | XP_011534269.1 | ||||
| XM_011535968.2 | Intron | XP_011534270.1 | ||||
| XM_011535969.2 | Intron | XP_011534271.1 | ||||
| XM_011535970.2 | Intron | XP_011534272.1 | ||||
| XM_011535971.2 | Intron | XP_011534273.1 | ||||
| XM_011535972.2 | Intron | XP_011534274.1 | ||||
| XM_011535973.2 | Intron | XP_011534275.1 | ||||
| XM_011535974.2 | Intron | XP_011534276.1 | ||||
| XM_011535976.1 | Intron | XP_011534278.1 | ||||
| XM_017011086.1 | Intron | XP_016866575.1 | ||||
| XM_017011087.1 | Intron | XP_016866576.1 | ||||
| XM_017011088.1 | Intron | XP_016866577.1 | ||||
| XM_017011089.1 | Intron | XP_016866578.1 | ||||
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