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CTCTCAGCAACATTTAGGACCAGTA[C/T]ATCGTGAAAAAGCCGAGATAATTAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 141180 | ||||||||||||||||||||
Literature Links: |
NCKAP1L 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 |
NCKAP1L - NCK associated protein 1 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001184976.1 | 182 | Missense Mutation | CAT,TAT | H,Y 28 | NP_001171905.1 | |
NM_005337.4 | 182 | Missense Mutation | CAT,TAT | H,Y 78 | NP_005328.2 |