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GAAGTGGCCGGCTGCAGGGACTGCA[C/T]GGTGAGGCAATCTGTGAGCAGGTCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610192 | ||||||||||||||||||||
Literature Links: |
GLIS3 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 |
GLIS3 - GLIS family zinc finger 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001042413.1 | 2099 | Missense Mutation | ATG,GTG | M,V 679 | NP_001035878.1 | |
NM_152629.3 | 2099 | Missense Mutation | ATG,GTG | M,V 524 | NP_689842.3 | |
XM_005251386.4 | 2099 | Missense Mutation | ATG,GTG | M,V 524 | XP_005251443.1 | |
XM_005251387.4 | 2099 | Missense Mutation | ATG,GTG | M,V 457 | XP_005251444.1 | |
XM_005251388.4 | 2099 | Missense Mutation | ATG,GTG | M,V 457 | XP_005251445.1 | |
XM_005251389.4 | 2099 | Intron | XP_005251446.1 | |||
XM_006716731.3 | 2099 | Intron | XP_006716794.1 | |||
XM_011517763.2 | 2099 | Missense Mutation | ATG,GTG | M,V 679 | XP_011516065.1 | |
XM_011517764.2 | 2099 | Missense Mutation | ATG,GTG | M,V 679 | XP_011516066.1 | |
XM_011517765.2 | 2099 | Missense Mutation | ATG,GTG | M,V 679 | XP_011516067.1 | |
XM_011517766.2 | 2099 | Missense Mutation | ATG,GTG | M,V 524 | XP_011516068.1 | |
XM_011517767.2 | 2099 | Missense Mutation | ATG,GTG | M,V 457 | XP_011516069.1 | |
XM_011517769.2 | 2099 | Intron | XP_011516071.1 | |||
XM_017014361.1 | 2099 | Missense Mutation | ATG,GTG | M,V 524 | XP_016869850.1 |
GLIS3-AS1 - GLIS3 antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |