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CCAGATGCCAGGCCCAGCTGTGCAC[C/T]GTCTGCCCAGCAGCTGGGAGCTGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 600853 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NDST1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
NDST1 - N-deacetylase and N-sulfotransferase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001301063.1 | 425 | Intron | NP_001287992.1 | |||
NM_001543.4 | 425 | Intron | NP_001534.1 | |||
XM_005268433.1 | 425 | Intron | XP_005268490.1 | |||
XM_005268434.2 | 425 | UTR 5 | XP_005268491.1 | |||
XM_005268435.4 | 425 | Intron | XP_005268492.1 | |||
XM_005268436.3 | 425 | Intron | XP_005268493.1 | |||
XM_005268437.4 | 425 | Intron | XP_005268494.1 | |||
XM_005268438.1 | 425 | Intron | XP_005268495.1 | |||
XM_005268439.1 | 425 | Intron | XP_005268496.1 | |||
XM_005268441.1 | 425 | Intron | XP_005268498.1 | |||
XM_005268442.3 | 425 | Intron | XP_005268499.1 | |||
XM_006714782.1 | 425 | Intron | XP_006714845.1 | |||
XM_006714783.1 | 425 | Intron | XP_006714846.1 | |||
XM_011537638.2 | 425 | Intron | XP_011535940.1 | |||
XM_017009427.1 | 425 | Intron | XP_016864916.1 | |||
XM_017009428.1 | 425 | Intron | XP_016864917.1 | |||
XM_017009429.1 | 425 | Intron | XP_016864918.1 | |||
XM_017009430.1 | 425 | Intron | XP_016864919.1 | |||
XM_017009431.1 | 425 | UTR 5 | XP_016864920.1 | |||
XM_017009432.1 | 425 | Intron | XP_016864921.1 | |||
XM_017009433.1 | 425 | Intron | XP_016864922.1 |