Product Details

SNP ID

rs10957154

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:60690402 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CATTTAATATTTTAATATTTGTCTT[A/G]ATTGTGTTAATTTTCAGAGCTGTGT

Phenotype

MIM: 608892

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CHD7 PubMed Links

Gene Details

Gene

CHD7

Gene Name

chromodomain helicase DNA binding protein 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001316690.1		Intron			NP_001303619.1
NM_017780.3		Intron			NP_060250.2
XM_011517553.2		Intron			XP_011515855.1
XM_011517554.2		Intron			XP_011515856.1
XM_011517555.2		Intron			XP_011515857.1
XM_011517560.2		Intron			XP_011515862.1
XM_017013612.1		Intron			XP_016869101.1
XM_017013613.1		Intron			XP_016869102.1

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