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TTTTTCTAGGTTTGAGCTGGCTGAA[G/T]AAGACGCGAAAGCAGGAAGAGGTCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 615052 MIM: 610350 | ||||||||||||||||||||
Literature Links: |
ASB7 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 |
ASB7 - ankyrin repeat and SOCS box containing 7 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024708.3 | 514 | UTR 5 | NP_078984.2 | |||
NM_198243.2 | 514 | UTR 5 | NP_937886.1 |
LINS1 - lines homolog 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040616.2 | 514 | Intron | NP_001035706.1 | |||
XM_005254941.1 | 514 | Intron | XP_005254998.1 | |||
XM_005254943.1 | 514 | Intron | XP_005255000.1 | |||
XM_017022398.1 | 514 | Intron | XP_016877887.1 | |||
XM_017022399.1 | 514 | Intron | XP_016877888.1 | |||
XM_017022400.1 | 514 | Intron | XP_016877889.1 |