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AGTGAAGAGGTAGAACTGGAGCTGC[C/T]CAGAGCTCTTATGAATCTGTTCTTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
7 submissions
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Phenotype: |
MIM: 608818 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NTNG1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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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NTNG1 - netrin G1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001113226.2 | Intron | NP_001106697.1 | ||||
NM_001113228.2 | Intron | NP_001106699.1 | ||||
NM_001312688.1 | Intron | NP_001299617.1 | ||||
NM_014917.3 | Intron | NP_055732.2 | ||||
XM_006710455.2 | Intron | XP_006710518.1 | ||||
XM_006710456.3 | Intron | XP_006710519.1 | ||||
XM_011541021.1 | Intron | XP_011539323.1 | ||||
XM_011541024.2 | Intron | XP_011539326.1 | ||||
XM_011541025.1 | Intron | XP_011539327.1 | ||||
XM_017000680.1 | Intron | XP_016856169.1 | ||||
XM_017000681.1 | Intron | XP_016856170.1 | ||||
XM_017000682.1 | Intron | XP_016856171.1 | ||||
XM_017000683.1 | Intron | XP_016856172.1 | ||||
XM_017000684.1 | Intron | XP_016856173.1 | ||||
XM_017000685.1 | Intron | XP_016856174.1 | ||||
XM_017000686.1 | Intron | XP_016856175.1 |