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AGAAGAGTTAAAATGGAATGCATCT[A/G]TAGATATATAGTTGGGAATGCGTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607978 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SAMSN1 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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SAMSN1 - SAM domain, SH3 domain and nuclear localization signals 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256370.1 | 1287 | UTR 3 | NP_001243299.1 | |||
NM_001286523.1 | 1287 | UTR 3 | NP_001273452.1 | |||
NM_022136.4 | 1287 | UTR 3 | NP_071419.3 | |||
XM_011529684.2 | 1287 | UTR 3 | XP_011527986.1 | |||
XM_011529685.1 | 1287 | UTR 3 | XP_011527987.1 | |||
XM_011529686.1 | 1287 | Intron | XP_011527988.1 | |||
XM_017028427.1 | 1287 | Intron | XP_016883916.1 |