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GGCCTCACGCCAACATGCAGGTCCT[C/G]CACCCCACGAGGCGGCAGCACGAAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
7 submissions
|
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Phenotype: |
MIM: 607215 | ||||||||||||||||||||
Literature Links: |
MIR4689 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 |
MIR4689 - microRNA 4689 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
NPHP4 - nephronophthisis 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001291593.1 | 3164 | Missense Mutation | CAG,GAG | Q,E 774 | NP_001278522.1 | |
NM_001291594.1 | 3164 | Missense Mutation | CAG,GAG | Q,E 775 | NP_001278523.1 | |
NM_015102.4 | 3164 | Missense Mutation | CAG,GAG | Q,E 1287 | NP_055917.1 | |
XM_006710563.3 | 3164 | Missense Mutation | CAG,GAG | Q,E 1287 | XP_006710626.1 | |
XM_011541213.1 | 3164 | Missense Mutation | CAG,GAG | Q,E 1286 | XP_011539515.1 | |
XM_011541214.1 | 3164 | Missense Mutation | CAG,GAG | Q,E 1273 | XP_011539516.1 | |
XM_011541215.1 | 3164 | Missense Mutation | CAG,GAG | Q,E 1250 | XP_011539517.1 | |
XM_011541216.2 | 3164 | Missense Mutation | CAG,GAG | Q,E 1287 | XP_011539518.1 | |
XM_011541217.2 | 3164 | Missense Mutation | CAG,GAG | Q,E 1287 | XP_011539519.1 | |
XM_011541218.2 | 3164 | Missense Mutation | CAG,GAG | Q,E 1287 | XP_011539520.1 | |
XM_017000996.1 | 3164 | Missense Mutation | CAG,GAG | Q,E 1272 | XP_016856485.1 | |
XM_017000997.1 | 3164 | Missense Mutation | CAG,GAG | Q,E 1287 | XP_016856486.1 | |
XM_017000998.1 | 3164 | Intron | XP_016856487.1 | |||
XM_017000999.1 | 3164 | Missense Mutation | CAG,GAG | Q,E 1111 | XP_016856488.1 | |
XM_017001000.1 | 3164 | Missense Mutation | CAG,GAG | Q,E 1111 | XP_016856489.1 | |
XM_017001001.1 | 3164 | Missense Mutation | CAG,GAG | Q,E 1021 | XP_016856490.1 | |
XM_017001002.1 | 3164 | Intron | XP_016856491.1 | |||
XM_017001003.1 | 3164 | Missense Mutation | CAG,GAG | Q,E 774 | XP_016856492.1 |