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Search Thermo Fisher Scientific
TGAGACTCCCTTTAGGTTGCATGGG[A/G]AAGACGTGACCCAGCTGACCAGGCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300561 MIM: 300565 | ||||||||||||||||||||
Literature Links: |
SLITRK2 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 |
SLITRK2 - SLIT and NTRK like family member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001144003.2 | 2197 | Missense Mutation | AAA,GAA | K,E 252 | NP_001137475.1 | |
NM_001144004.2 | 2197 | Missense Mutation | AAA,GAA | K,E 252 | NP_001137476.1 | |
NM_001144005.2 | 2197 | Missense Mutation | AAA,GAA | K,E 252 | NP_001137477.1 | |
NM_001144006.2 | 2197 | Missense Mutation | AAA,GAA | K,E 252 | NP_001137478.1 | |
NM_001144008.2 | 2197 | Missense Mutation | AAA,GAA | K,E 252 | NP_001137480.1 | |
NM_001144009.2 | 2197 | Missense Mutation | AAA,GAA | K,E 252 | NP_001137481.1 | |
NM_001144010.2 | 2197 | Missense Mutation | AAA,GAA | K,E 252 | NP_001137482.1 | |
NM_032539.4 | 2197 | Missense Mutation | AAA,GAA | K,E 252 | NP_115928.1 | |
XM_005262342.3 | 2197 | Missense Mutation | AAA,GAA | K,E 252 | XP_005262399.1 | |
XM_005262343.3 | 2197 | Missense Mutation | AAA,GAA | K,E 252 | XP_005262400.1 | |
XM_005262344.3 | 2197 | Missense Mutation | AAA,GAA | K,E 252 | XP_005262401.1 | |
XM_005262345.3 | 2197 | Missense Mutation | AAA,GAA | K,E 252 | XP_005262402.1 |
TMEM257 - transmembrane protein 257 | ||||||
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There are no transcripts associated with this gene. |