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AAGACATAAGGAAAACAAGATTCCA[A/G]AAGATCCATTGTAAGGAATGGAGAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604891 | ||||||||||||||||||||
Literature Links: |
NCKAP1 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 |
NCKAP1 - NCK associated protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_013436.4 | 3554 | Silent Mutation | CTG,TTG | L,L 1103 | NP_038464.1 | |
NM_205842.2 | 3554 | Silent Mutation | CTG,TTG | L,L 1109 | NP_995314.1 | |
XM_006712200.3 | 3554 | Silent Mutation | CTG,TTG | L,L 1107 | XP_006712263.1 | |
XM_006712201.3 | 3554 | Silent Mutation | CTG,TTG | L,L 1101 | XP_006712264.1 |