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AATACCAGAAGCTGCGTTGTCATTG[A/G]TGAAGGAATATTTCGAAGCGCTGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
MIM: 615406 MIM: 611514 | ||||||||||||||||||||
Literature Links: |
GNG12-AS1 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 |
GNG12-AS1 - GNG12 antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |
WLS - wntless Wnt ligand secretion mediator | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001002292.3 | 1845 | Missense Mutation | ACC,ATC | T,I 535 | NP_001002292.3 | |
NM_001193334.1 | 1845 | Intron | NP_001180263.1 | |||
NM_024911.6 | 1845 | Intron | NP_079187.3 | |||
XM_011542191.2 | 1845 | Missense Mutation | ACC,ATC | T,I 537 | XP_011540493.1 | |
XM_011542192.2 | 1845 | Missense Mutation | ACC,ATC | T,I 492 | XP_011540494.1 | |
XM_017002390.1 | 1845 | Intron | XP_016857879.1 |