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TGTATATTCCTGGGAATATTTTTCT[A/G]AGATATTTCCAGAATGAAATTGCTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600016 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CNTN1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
CNTN1 - contactin 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256063.1 | Intron | NP_001242992.1 | ||||
NM_001256064.1 | Intron | NP_001242993.1 | ||||
NM_001843.3 | Intron | NP_001834.2 | ||||
NM_175038.2 | Intron | NP_778203.1 | ||||
XM_005268651.2 | Intron | XP_005268708.1 | ||||
XM_006719241.2 | Intron | XP_006719304.1 | ||||
XM_011537926.2 | Intron | XP_011536228.1 | ||||
XM_011537927.2 | Intron | XP_011536229.1 | ||||
XM_017018821.1 | Intron | XP_016874310.1 | ||||
XM_017018822.1 | Intron | XP_016874311.1 | ||||
XM_017018823.1 | Intron | XP_016874312.1 | ||||
XM_017018824.1 | Intron | XP_016874313.1 | ||||
XM_017018825.1 | Intron | XP_016874314.1 | ||||
XM_017018826.1 | Intron | XP_016874315.1 | ||||
XM_017018827.1 | Intron | XP_016874316.1 |