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ATCGCGCTGTGCAGATCCCTCAGCA[A/T]ATTGTGACAGTATTATGGCACTTTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610348 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLF2 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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SLF2 - SMC5-SMC6 complex localization factor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001136123.1 | 2262 | Intron | NP_001129595.1 | |||
NM_001243770.1 | 2262 | Intron | NP_001230699.1 | |||
NM_018121.3 | 2262 | Intron | NP_060591.3 | |||
XM_005269965.2 | 2262 | Intron | XP_005270022.1 | |||
XM_011539944.2 | 2262 | UTR 5 | XP_011538246.1 |