Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAAGGTGATGCGCCTGAAGGACTAC[A/G]TCAAGGTGAAGGTGGAGCCCTCAGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
NTNG2 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 |
NTNG2 - netrin G2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032536.2 | 945 | Missense Mutation | ATC,GTC | I,V 50 | NP_115925.2 | |
XM_006717304.3 | 945 | Missense Mutation | ATC,GTC | I,V 50 | XP_006717367.1 | |
XM_011519094.2 | 945 | Missense Mutation | ATC,GTC | I,V 50 | XP_011517396.1 | |
XM_011519096.2 | 945 | Missense Mutation | ATC,GTC | I,V 50 | XP_011517398.1 | |
XM_011519097.2 | 945 | Missense Mutation | ATC,GTC | I,V 50 | XP_011517399.1 | |
XM_011519098.2 | 945 | Missense Mutation | ATC,GTC | I,V 50 | XP_011517400.1 | |
XM_011519099.2 | 945 | Missense Mutation | ATC,GTC | I,V 50 | XP_011517401.1 | |
XM_011519100.2 | 945 | Missense Mutation | ATC,GTC | I,V 50 | XP_011517402.1 | |
XM_011519102.2 | 945 | Missense Mutation | ATC,GTC | I,V 50 | XP_011517404.1 | |
XM_011519103.2 | 945 | Missense Mutation | ATC,GTC | I,V 50 | XP_011517405.1 | |
XM_011519104.2 | 945 | Missense Mutation | ATC,GTC | I,V 50 | XP_011517406.1 | |
XM_011519105.2 | 945 | Missense Mutation | ATC,GTC | I,V 50 | XP_011517407.1 | |
XM_011519106.2 | 945 | Missense Mutation | ATC,GTC | I,V 50 | XP_011517408.1 | |
XM_011519107.2 | 945 | Missense Mutation | ATC,GTC | I,V 50 | XP_011517409.1 | |
XM_011519108.2 | 945 | Missense Mutation | ATC,GTC | I,V 50 | XP_011517410.1 | |
XM_011519109.2 | 945 | Missense Mutation | ATC,GTC | I,V 50 | XP_011517411.1 | |
XM_011519110.2 | 945 | Missense Mutation | ATC,GTC | I,V 50 | XP_011517412.1 | |
XM_011519112.2 | 945 | Intron | XP_011517414.1 | |||
XM_011519113.2 | 945 | Intron | XP_011517415.1 | |||
XM_017015212.1 | 945 | Missense Mutation | ATC,GTC | I,V 50 | XP_016870701.1 | |
XM_017015213.1 | 945 | Missense Mutation | ATC,GTC | I,V 50 | XP_016870702.1 | |
XM_017015214.1 | 945 | Missense Mutation | ATC,GTC | I,V 50 | XP_016870703.1 | |
XM_017015215.1 | 945 | Intron | XP_016870704.1 | |||
XM_017015216.1 | 945 | Missense Mutation | ATC,GTC | I,V 50 | XP_016870705.1 |