Product Details

SNP ID

rs78613619

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:88463979 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGTATAGAGTGACTCAGATAGCAT[C/G]TGGAAGGTAAGTTGTAAAGTATCAA

Phenotype

MIM: 608242

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

HERC5 PubMed Links

Gene Details

Gene

HERC5

Gene Name

HECT and RLD domain containing E3 ubiquitin protein ligase 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016323.3	1571	Missense Mutation	TCT,TGT	S302C	NP_057407.2
XM_011532022.2	1571	Missense Mutation	TCT,TGT	S453C	XP_011530324.2

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