Product Details

SNP ID
rs28373720
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.15:74210256 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATATGGAGACAAAATTCCCAAGGCC[A/G]TTTGTAATGGCAAAAATAATTGGCA
Phenotype
MIM: 610745
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
CCDC33 PubMed Links

Gene Details

Gene
CCDC33
Gene Name
coiled-coil domain containing 33
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001287181.1 Intron NP_001274110.1
NM_025055.4 Intron NP_079331.3
NM_182791.3 Intron NP_877592.2
XM_005254692.1 Intron XP_005254749.1
XM_011522085.2 Intron XP_011520387.1
XM_011522086.1 Intron XP_011520388.1
XM_011522087.2 Intron XP_011520389.1
XM_011522088.1 Intron XP_011520390.1
XM_011522089.2 Intron XP_011520391.1
XM_011522090.2 Intron XP_011520392.2
XM_017022623.1 Intron XP_016878112.1
XM_017022624.1 Intron XP_016878113.1
XM_017022625.1 Intron XP_016878114.1
XM_017022626.1 Intron XP_016878115.1
XM_017022627.1 Intron XP_016878116.1
XM_017022628.1 Intron XP_016878117.1
XM_017022629.1 Intron XP_016878118.1
XM_017022630.1 Intron XP_016878119.1
XM_017022631.1 Intron XP_016878120.1
XM_017022632.1 Intron XP_016878121.1
XM_017022633.1 Intron XP_016878122.1
Gene
STRA6
Gene Name
stimulated by retinoic acid 6
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001142617.1 Intron NP_001136089.1
NM_001142618.1 Intron NP_001136090.1
NM_001142619.1 Intron NP_001136091.1
NM_001142620.1 Intron NP_001136092.1
NM_001199040.1 Intron NP_001185969.1
NM_001199041.1 Intron NP_001185970.1
NM_001199042.1 Intron NP_001185971.1
NM_022369.3 Intron NP_071764.3
XM_011521883.1 Intron XP_011520185.1
XM_011521884.1 Intron XP_011520186.1
XM_011521885.2 Intron XP_011520187.1
XM_017022478.1 Intron XP_016877967.1
XM_017022479.1 Intron XP_016877968.1
XM_017022480.1 Intron XP_016877969.1

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