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GTCCCTCCGCGAAACTCCCTGAGCA[C/G]TGGGTGTGAAGGGCAGCGGCGCCCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608582 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
EGFL7 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
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CEPH (CEU) - Not Available | ||||||
EAS
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African American
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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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EGFL7 - EGF like domain multiple 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016215.4 | Intron | NP_057299.1 | ||||
NM_201446.2 | Intron | NP_958854.1 | ||||
XM_006717141.3 | Intron | XP_006717204.1 | ||||
XM_011518764.1 | Intron | XP_011517066.1 | ||||
XM_011518765.1 | Intron | XP_011517067.1 | ||||
XM_011518766.1 | Intron | XP_011517068.1 | ||||
XM_011518767.1 | Intron | XP_011517069.1 | ||||
XM_011518768.1 | Intron | XP_011517070.1 | ||||
XM_017014795.1 | Intron | XP_016870284.1 | ||||
XM_017014796.1 | Intron | XP_016870285.1 | ||||
XM_017014797.1 | Intron | XP_016870286.1 | ||||
XM_017014798.1 | Intron | XP_016870287.1 | ||||
XM_017014799.1 | Intron | XP_016870288.1 |
HSPC324 - uncharacterized LOC101928612 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
Validated |