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TCTGGGGGTGGCGGGCGAAGGCGTA[A/G]GCCTGCCCCAGGATGGCCAGGTCCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605696 | ||||||||||||||||||||
Literature Links: |
KCNG2 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 |
KCNG2 - potassium voltage-gated channel modifier subfamily G member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_012283.1 | 786 | Intron | NP_036415.1 |
PQLC1 - PQ loop repeat containing 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001146343.1 | 786 | UTR 3 | NP_001139815.1 | |||
NM_001146345.1 | 786 | Silent Mutation | GCC,GCT | A,A 230 | NP_001139817.1 | |
NM_025078.4 | 786 | Silent Mutation | GCC,GCT | A,A 248 | NP_079354.2 | |
XM_005266770.2 | 786 | UTR 3 | XP_005266827.1 | |||
XM_011526188.1 | 786 | Silent Mutation | GCC,GCT | A,A 130 | XP_011524490.1 | |
XM_017025997.1 | 786 | Silent Mutation | GCC,GCT | A,A 273 | XP_016881486.1 | |
XM_017025998.1 | 786 | Silent Mutation | GCC,GCT | A,A 255 | XP_016881487.1 | |
XM_017025999.1 | 786 | Intron | XP_016881488.1 | |||
XM_017026000.1 | 786 | Intron | XP_016881489.1 | |||
XM_017026001.1 | 786 | Silent Mutation | GCC,GCT | A,A 167 | XP_016881490.1 | |
XM_017026002.1 | 786 | Intron | XP_016881491.1 | |||
XM_017026003.1 | 786 | UTR 3 | XP_016881492.1 | |||
XM_017026004.1 | 786 | UTR 3 | XP_016881493.1 | |||
XM_017026005.1 | 786 | Silent Mutation | GCC,GCT | A,A 130 | XP_016881494.1 |