Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCAGTGAAGCCATTTTTGCAGTTGG[A/G]GGTGTAAGCTGAAAAATCTTTCCTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605358 MIM: 152790 | ||||||||||||||||||||
Literature Links: |
GTF2A1L 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 |
GTF2A1L - general transcription factor IIA subunit 1 like | ||||||
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There are no transcripts associated with this gene. |
LHCGR - luteinizing hormone/choriogonadotropin receptor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000233.3 | 1777 | Missense Mutation | NP_000224.2 | |||
XM_005264309.3 | 1777 | Missense Mutation | XP_005264366.1 | |||
XM_006712015.3 | 1777 | Missense Mutation | XP_006712078.1 | |||
XM_011532828.1 | 1777 | Missense Mutation | XP_011531130.1 | |||
XM_011532831.1 | 1777 | Missense Mutation | XP_011531133.1 | |||
XM_011532834.2 | 1777 | Missense Mutation | XP_011531136.1 | |||
XM_017004089.1 | 1777 | Missense Mutation | XP_016859578.1 | |||
XM_017004090.1 | 1777 | Missense Mutation | XP_016859579.1 |
STON1-GTF2A1L - STON1-GTF2A1L readthrough | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001198593.1 | 1777 | Intron | NP_001185522.1 | |||
NM_001198594.1 | 1777 | Intron | NP_001185523.1 | |||
NM_172311.2 | 1777 | Intron | NP_758515.1 |