Product Details

SNP ID

rs202216099

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:39133930 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCGGTCTCGGAAGAAGCCCTCAGC[C/T]GCCTGGGCCTCGCGGAAGGTGACGG

Phenotype

MIM: 608457

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CBX7 PubMed Links

Gene Details

Gene

CBX7

Gene Name

chromobox 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_175709.3	750	Silent Mutation	GCA,GCG	A239A	NP_783640.1
XM_005261413.4	750	Silent Mutation	GCA,GCG	A146A	XP_005261470.1
XM_006724174.3	750	Silent Mutation	GCA,GCG	A247A	XP_006724237.1
XM_006724175.3	750	Silent Mutation	GCA,GCG	A246A	XP_006724238.1
XM_006724176.3	750	Silent Mutation	GCA,GCG	A188A	XP_006724239.1
XM_006724177.3	750	Silent Mutation	GCA,GCG	A180A	XP_006724240.1
XM_006724178.3	750	Silent Mutation	GCA,GCG	A154A	XP_006724241.1
XM_011530025.2	750	Silent Mutation	GCA,GCG	A153A	XP_011528327.1
XM_017028679.1	750	Silent Mutation	GCA,GCG	A238A	XP_016884168.1

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