Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGGCAAGGGTCTGTGACACAGCGC[A/G]GGCAGCACTCATTCTCTGGGAGAAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602320 | ||||||||||||||||||||
Literature Links: |
NELL2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
NELL2 - neural EGFL like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145107.1 | 2533 | Missense Mutation | CCG,CTG | P,L 803 | NP_001138579.1 | |
NM_001145108.1 | 2533 | Missense Mutation | CCG,CTG | P,L 753 | NP_001138580.1 | |
NM_001145109.1 | 2533 | Missense Mutation | CCG,CTG | P,L 752 | NP_001138581.1 | |
NM_001145110.1 | 2533 | Missense Mutation | CCG,CTG | P,L 776 | NP_001138582.1 | |
NM_006159.2 | 2533 | Missense Mutation | CCG,CTG | P,L 753 | NP_006150.1 | |
XM_005268905.3 | 2533 | Missense Mutation | CCG,CTG | P,L 753 | XP_005268962.1 | |
XM_011538396.1 | 2533 | Missense Mutation | CCG,CTG | P,L 753 | XP_011536698.1 | |
XM_017019341.1 | 2533 | Missense Mutation | CCG,CTG | P,L 808 | XP_016874830.1 | |
XM_017019342.1 | 2533 | Missense Mutation | CCG,CTG | P,L 758 | XP_016874831.1 | |
XM_017019343.1 | 2533 | Missense Mutation | CCG,CTG | P,L 758 | XP_016874832.1 | |
XM_017019344.1 | 2533 | Missense Mutation | CCG,CTG | P,L 758 | XP_016874833.1 |