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SNP ID: rs1064285
Assay Type: Functionally tested
NCBI dbSNP Submissions: 5
Location: Chr.1:6102114 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TGCTCCCTCCACACCCCTGAACTCA[A/G]ACCCCACGGGCCAGTGGGGACCCTC
Phenotype: MIM: 610771 MIM: 601142
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: CHD5 PubMed Links

Gene Details

Gene: CHD5
Gene Name: chromodomain helicase DNA binding protein 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015557.2	9336	UTR 3			NP_056372.1

Gene: KCNAB2
Gene Name: potassium voltage-gated channel subfamily A regulatory beta subunit 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001199860.1	9336	Intron			NP_001186789.1
NM_001199861.1	9336	Intron			NP_001186790.1
NM_001199862.1	9336	Intron			NP_001186791.1
NM_001199863.1	9336	Intron			NP_001186792.1
NM_003636.3	9336	Intron			NP_003627.1
NM_172130.2	9336	Intron			NP_742128.1
XM_005263514.2	9336	Intron			XP_005263571.1
XM_011542321.2	9336	Intron			XP_011540623.1
XM_011542322.2	9336	Intron			XP_011540624.1
XM_017002618.1	9336	Intron			XP_016858107.1
XM_017002619.1	9336	Intron			XP_016858108.1
XM_017002620.1	9336	Intron			XP_016858109.1
XM_017002621.1	9336	Intron			XP_016858110.1

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