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ATGCTCATTTGAAAACAGACAACGT[A/G]TCTAAAGATGTATAGAGTGATTGGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607866 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SPRYD7 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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SPRYD7 - SPRY domain containing 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001127482.2 | 1838 | UTR 3 | NP_001120954.1 | |||
NM_020456.3 | 1838 | UTR 3 | NP_065189.1 | |||
XM_017020677.1 | 1838 | Intron | XP_016876166.1 |