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SNP ID: rs1043006
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.20:35953776 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGTGATGCGCACATCCGTGCGGCGG[G/C]GGATCCGCCGGGCCCGAGCCGCCTC
Phenotype: MIM: 610335 MIM: 610416
Polymorphism: G/C, Transversion 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	743	Intron			NP_001194005.1
NM_001304367.1	743	Intron			NP_001291296.1
NM_080834.3	743	Intron			NP_543024.2
XM_005260295.2	743	Intron			XP_005260352.1
XM_011528590.2	743	Intron			XP_011526892.1
XM_011528592.1	743	Intron			XP_011526894.1
XM_011528593.2	743	Intron			XP_011526895.1
XM_011528598.1	743	Intron			XP_011526900.1
XM_017027683.1	743	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	743	Missense Mutation	CCC,CGC	P170R	NP_057642.1
NM_033630.2	743	Missense Mutation	CCC,CGC	P233R	NP_361012.2

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