Product Details

SNP ID

rs3027877

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:153952750 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGTGGGGGTGGCTGGACCACCACA[C/G]TGGCCACCACCGCAGAGCCGGCAGA

Phenotype

MIM: 300019 MIM: 312420

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

HCFC1 PubMed Links

Gene Details

Gene

HCFC1

Gene Name

host cell factor C1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005334.2	5699	Missense Mutation	ACT,AGT	T1569S	NP_005325.2
XM_006724815.2	5699	Missense Mutation	ACT,AGT	T1613S	XP_006724878.1
XM_006724816.2	5699	Missense Mutation	ACT,AGT	T1613S	XP_006724879.1
XM_011531147.2	5699	Missense Mutation	ACT,AGT	T1569S	XP_011529449.1
XM_011531148.2	5699	Missense Mutation	ACT,AGT	T1569S	XP_011529450.1
XM_017029471.1	5699	Missense Mutation	ACT,AGT	T1547S	XP_016884960.1
XM_017029472.1	5699	Missense Mutation	ACT,AGT	T1310S	XP_016884961.1

Gene

RENBP

Gene Name

renin binding protein

There are no transcripts associated with this gene.

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