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AGTGGACTGTCACGGGCTGGCGCTG[A/C]GCAGCGTGCCCAGGAATATCCCCCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603746 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLIT2 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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SLIT2 - slit guidance ligand 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001289135.2 | 2050 | Missense Mutation | AGC,CGC | S,R 47 | NP_001276064.1 | |
NM_001289136.2 | 2050 | Missense Mutation | AGC,CGC | S,R 47 | NP_001276065.1 | |
NM_004787.3 | 2050 | Missense Mutation | AGC,CGC | S,R 47 | NP_004778.1 | |
XM_005248211.3 | 2050 | Missense Mutation | AGC,CGC | S,R 47 | XP_005248268.1 | |
XM_006713986.3 | 2050 | Missense Mutation | AGC,CGC | S,R 47 | XP_006714049.1 | |
XM_011513909.2 | 2050 | Intron | XP_011512211.1 | |||
XM_011513910.2 | 2050 | Intron | XP_011512212.2 | |||
XM_017008845.1 | 2050 | Intron | XP_016864334.1 |