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CTTCCCCACCATCCACCTCAGAAGC[A/G]GTCCCAGCCTGCCACCCGCCAGCCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
MIM: 611275 | ||||||||||||||||||||
Literature Links: |
BNIPL 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 |
BNIPL - BCL2 interacting protein like | ||||||
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There are no transcripts associated with this gene. |
C1orf56 - chromosome 1 open reading frame 56 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_017860.3 | 954 | Missense Mutation | AGT,GGT | S,G 297 | NP_060330.2 |
CDC42SE1 - CDC42 small effector 1 | ||||||
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There are no transcripts associated with this gene. |