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TGGGGAAAGAGTCCATACAGATGGT[A/C]GTCCATTCAGATGGTTGTGGGGGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602965 MIM: 610728 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FABP7 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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FABP7 - fatty acid binding protein 7 | ||||||
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There are no transcripts associated with this gene. |
SMPDL3A - sphingomyelin phosphodiesterase acid like 3A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286138.1 | 499 | Intron | NP_001273067.1 | |||
NM_006714.4 | 499 | Intron | NP_006705.1 | |||
XM_005266797.4 | 499 | Intron | XP_005266854.1 | |||
XM_005266798.2 | 499 | Intron | XP_005266855.1 | |||
XM_005266799.2 | 499 | Intron | XP_005266856.1 | |||
XM_005266801.2 | 499 | Intron | XP_005266858.1 | |||
XM_005266802.2 | 499 | UTR 5 | XP_005266859.1 | |||
XM_017010203.1 | 499 | Intron | XP_016865692.1 | |||
XM_017010204.1 | 499 | Intron | XP_016865693.1 |