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TCCTTGTCGGCCACATTTCTCATAA[A/C]AACTTTCTGTCCTGGAGGATCTGAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300562 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLITRK4 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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SLITRK4 - SLIT and NTRK like family member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001184749.2 | 2334 | Missense Mutation | GTT,TTT | V,F 720 | NP_001171678.1 | |
NM_001184750.2 | 2334 | Missense Mutation | GTT,TTT | V,F 720 | NP_001171679.1 | |
NM_173078.4 | 2334 | Missense Mutation | GTT,TTT | V,F 720 | NP_775101.1 | |
XM_005262365.4 | 2334 | Missense Mutation | GTT,TTT | V,F 720 | XP_005262422.1 | |
XM_011531265.2 | 2334 | Missense Mutation | GTT,TTT | V,F 720 | XP_011529567.1 |