Product Details

SNP ID

rs200110333

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:56648758 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATCTGCACTCTGAGGGCAGGCCTT[C/G]TGAGCGCCGCCACTTTGCCAGGCGC

Phenotype

MIM: 607275

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

HOPX PubMed Links

Gene Details

Gene

HOPX

Gene Name

HOP homeobox

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145459.1	651	Missense Mutation	CAA,GAA	Q62E	NP_001138931.1
NM_001145460.1	651	UTR 3			NP_001138932.1
NM_032495.5	651	Missense Mutation	CAA,GAA	Q80E	NP_115884.4
NM_139211.4	651	Missense Mutation	CAA,GAA	Q62E	NP_631957.1
NM_139212.3	651	Missense Mutation	CAA,GAA	Q62E	NP_631958.1
XM_006714052.2	651	Intron			XP_006714115.1
XM_017008728.1	651	Missense Mutation	CAA,GAA	Q77E	XP_016864217.1
XM_017008729.1	651	Missense Mutation	CAA,GAA	Q62E	XP_016864218.1
XM_017008730.1	651	Missense Mutation	CAA,GAA	Q62E	XP_016864219.1
XM_017008731.1	651	Missense Mutation	CAA,GAA	Q62E	XP_016864220.1
XM_017008732.1	651	Missense Mutation	CAA,GAA	Q62E	XP_016864221.1
XM_017008733.1	651	Missense Mutation	CAA,GAA	Q62E	XP_016864222.1
XM_017008734.1	651	Missense Mutation	CAA,GAA	Q62E	XP_016864223.1

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