Product Details

SNP ID: rs61757401
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:42797936 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GTCCCTGGTTTCTTGGGCTCAATCA[C/G]GGTCCAAGGTTAGTAAGAAGGCCAA
Phenotype: MIM: 614775 MIM: 601844
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: CNTD1 PubMed Links

Gene Details

Gene: CNTD1
Gene Name: cyclin N-terminal domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173478.2	490	Intron			NP_775749.2
XM_005257043.4	490	Intron			XP_005257100.1
XM_005257044.4	490	Intron			XP_005257101.1
XM_005257045.4	490	Intron			XP_005257102.1
XM_006721690.2	490	Intron			XP_006721753.1
XM_011524310.2	490	Intron			XP_011522612.1
XM_011524311.2	490	Intron			XP_011522613.1
XM_017024171.1	490	Intron			XP_016879660.1

Gene: COA3
Gene Name: cytochrome c oxidase assembly factor 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001040431.2	490	UTR 3			NP_001035521.1

Gene: WNK4
Gene Name: WNK lysine deficient protein kinase 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001321299.1	490	Intron			NP_001308228.1
NM_032387.4	490	Intron			NP_115763.2
XM_011525135.2	490	Intron			XP_011523437.1
XM_017024962.1	490	Intron			XP_016880451.1
XM_017024963.1	490	Intron			XP_016880452.1
XM_017024964.1	490	Intron			XP_016880453.1
XM_017024965.1	490	Intron			XP_016880454.1
XM_017024966.1	490	Intron			XP_016880455.1

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