Product Details

SNP ID: rs11538234
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.20:35953849 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TCTTGCACCAGCATCTCCACGATCT[A/G]CTCCTTGGTGCGGATGTCAGGCCGC
Phenotype: MIM: 610335 MIM: 610416
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: CNBD2 PubMed Links

Gene Details

Gene: CNBD2
Gene Name: cyclic nucleotide binding domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001207076.2	670	Intron			NP_001194005.1
NM_001304367.1	670	Intron			NP_001291296.1
NM_080834.3	670	Intron			NP_543024.2
XM_005260295.2	670	Intron			XP_005260352.1
XM_011528590.2	670	Intron			XP_011526892.1
XM_011528592.1	670	Intron			XP_011526894.1
XM_011528593.2	670	Intron			XP_011526895.1
XM_011528598.1	670	Intron			XP_011526900.1
XM_017027683.1	670	Intron			XP_016883172.1

Gene: PHF20
Gene Name: PHD finger protein 20

There are no transcripts associated with this gene.

Gene: SCAND1
Gene Name: SCAN domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016558.3	670	Nonsense Mutation	CAG,TAG	Q146*	NP_057642.1
NM_033630.2	670	Nonsense Mutation	CAG,TAG	Q209*	NP_361012.2

View Full Product Details