Product Details

SNP ID
rs61739903
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:74949399 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGGCCGTAGCGGCTTGTTGGATAA[C/G]GTGAGGAGCCGGTTCTTGGGAACAG
Phenotype
MIM: 609788
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
SPCS2 PubMed Links

Gene Details

Gene
SPCS2
Gene Name
signal peptidase complex subunit 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014752.2 153 Missense Mutation AAC,AAG N38K NP_055567.2
Gene
XRRA1
Gene Name
X-ray radiation resistance associated 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001270380.1 153 Intron NP_001257309.1
NM_001270381.1 153 Intron NP_001257310.1
NM_182969.2 153 Intron NP_892014.1
XM_005273765.2 153 Intron XP_005273822.1
XM_005273770.2 153 Intron XP_005273827.1
XM_011544755.1 153 Intron XP_011543057.1
XM_011544756.1 153 Intron XP_011543058.1
XM_011544757.1 153 Intron XP_011543059.1
XM_011544758.1 153 Intron XP_011543060.1
XM_011544759.1 153 Intron XP_011543061.1
XM_011544760.2 153 Intron XP_011543062.1
XM_011544761.1 153 Intron XP_011543063.1
XM_011544762.1 153 Intron XP_011543064.1
XM_011544763.1 153 Intron XP_011543065.1
XM_011544764.1 153 Intron XP_011543066.1
XM_011544765.1 153 Intron XP_011543067.1
XM_011544766.2 153 Intron XP_011543068.1
XM_011544767.1 153 Intron XP_011543069.1
XM_011544768.1 153 Intron XP_011543070.1
XM_017017221.1 153 Intron XP_016872710.1
XM_017017222.1 153 Intron XP_016872711.1
XM_017017223.1 153 Intron XP_016872712.1
XM_017017224.1 153 Intron XP_016872713.1
XM_017017225.1 153 Intron XP_016872714.1
XM_017017226.1 153 Intron XP_016872715.1
XM_017017227.1 153 Intron XP_016872716.1
XM_017017228.1 153 Intron XP_016872717.1
XM_017017229.1 153 Intron XP_016872718.1
XM_017017230.1 153 Intron XP_016872719.1
XM_017017231.1 153 Intron XP_016872720.1
XM_017017232.1 153 Intron XP_016872721.1
XM_017017233.1 153 Intron XP_016872722.1
XM_017017234.1 153 Intron XP_016872723.1

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