Product Details

SNP ID
rs151194260
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.18:79902497 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCAGTCACTGCGCCTGCAGTCGGC[A/G]ACAGTTTAATGTGAGGCAATTACCG
Phenotype
MIM: 605696
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
KCNG2 PubMed Links

Gene Details

Gene
KCNG2
Gene Name
potassium voltage-gated channel modifier subfamily G member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_012283.1 2337 Intron NP_036415.1
XM_011525918.2 2337 Intron XP_011524220.1
XM_011525920.2 2337 Intron XP_011524222.1
XM_017025704.1 2337 Intron XP_016881193.1
XM_017025705.1 2337 Intron XP_016881194.1
Gene
PQLC1
Gene Name
PQ loop repeat containing 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001146343.1 2337 UTR 3 NP_001139815.1
NM_001146345.1 2337 UTR 3 NP_001139817.1
NM_025078.4 2337 UTR 3 NP_079354.2
XM_005266770.2 2337 UTR 3 XP_005266827.1
XM_011526188.1 2337 UTR 3 XP_011524490.1
XM_017025997.1 2337 UTR 3 XP_016881486.1
XM_017025998.1 2337 UTR 3 XP_016881487.1
XM_017025999.1 2337 Intron XP_016881488.1
XM_017026000.1 2337 Intron XP_016881489.1
XM_017026001.1 2337 UTR 3 XP_016881490.1
XM_017026002.1 2337 Intron XP_016881491.1
XM_017026003.1 2337 UTR 3 XP_016881492.1
XM_017026004.1 2337 UTR 3 XP_016881493.1
XM_017026005.1 2337 UTR 3 XP_016881494.1

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