Product Details

SNP ID

rs7503751

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:7886224 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCCCCGAGGTGACAAGTCACCCGGC[A/G]GCACTCTCTGGGCGGCGCTCTCCAG

Phenotype

MIM: 602120

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CHD3 PubMed Links

Gene Details

Gene

CHD3

Gene Name

chromodomain helicase DNA binding protein 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001005271.2		Intron			NP_001005271.2
NM_001005273.2		Intron			NP_001005273.1
NM_005852.3		Intron			NP_005843.2
XM_005256427.4		Intron			XP_005256484.1
XM_005256428.4		Intron			XP_005256485.1
XM_005256429.4		Intron			XP_005256486.1
XM_005256431.4		Intron			XP_005256488.1
XM_006721423.3		Intron			XP_006721486.1
XM_006721424.3		Intron			XP_006721487.1
XM_006721428.3		Intron			XP_006721491.1
XM_017024061.1		Intron			XP_016879550.1
XM_017024062.1		Intron			XP_016879551.1
XM_017024063.1		Intron			XP_016879552.1
XM_017024064.1		Intron			XP_016879553.1
XM_017024065.1		Intron			XP_016879554.1
XM_017024066.1		Intron			XP_016879555.1
XM_017024067.1		Intron			XP_016879556.1
XM_017024068.1		Intron			XP_016879557.1
XM_017024069.1		Intron			XP_016879558.1
XM_017024070.1		Intron			XP_016879559.1

Gene

NAA38

Gene Name

N(alpha)-acetyltransferase 38, NatC auxiliary subunit

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_011524037.2		Intron			XP_011522339.1
XM_017025225.1		Intron			XP_016880714.1
XM_017025226.1		Intron			XP_016880715.1

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