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SNP ID: rs11699815
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.20:35955203 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CTCAGCTCTTGCAACGTAGCTAGTT[A/G]ATAACCCTCGAAATATAGCGAATTG
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	157	Intron			NP_001194005.1
NM_001304367.1	157	Intron			NP_001291296.1
NM_080834.3	157	Intron			NP_543024.2
XM_005260295.2	157	Intron			XP_005260352.1
XM_011528590.2	157	Intron			XP_011526892.1
XM_011528592.1	157	Intron			XP_011526894.1
XM_011528593.2	157	Intron			XP_011526895.1
XM_011528598.1	157	Intron			XP_011526900.1
XM_017027683.1	157	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	157	UTR 5			NP_057642.1
NM_033630.2	157	Intron			NP_361012.2

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