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CCCAGTTTGAAGGCCAGCATGCAGG[A/G]GGAATTCTCTCTTGCTCAGGGAATG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 604242 | ||||||||||||||||||||
Literature Links: |
RNF6 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 |
RNF6 - ring finger protein 6 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005977.3 | Intron | NP_005968.1 | ||||
NM_183043.2 | Intron | NP_898864.1 | ||||
NM_183044.2 | Intron | NP_898865.1 | ||||
NM_183045.1 | Intron | NP_898866.1 | ||||
XM_005266485.2 | Intron | XP_005266542.1 | ||||
XM_005266486.2 | Intron | XP_005266543.1 | ||||
XM_011535177.2 | Intron | XP_011533479.1 | ||||
XM_011535178.1 | Intron | XP_011533480.1 | ||||
XM_017020685.1 | Intron | XP_016876174.1 | ||||
XM_017020686.1 | Intron | XP_016876175.1 | ||||
XM_017020687.1 | Intron | XP_016876176.1 |