Product Details

SNP ID

rs3734928

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:130070648 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGCGGCAATCGTTAGCGGGTCATGT[C/T]GGCCGCCCAGGGCTGGGACAGGAAC

Phenotype

MIM: 615152

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

KLHDC10 PubMed Links

Gene Details

Gene

KLHDC10

Gene Name

kelch domain containing 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014997.3	116	Missense Mutation	TCG,TTG	S2L	NP_055812.1
XM_005250233.4	116	Missense Mutation	TCG,TTG	S2L	XP_005250290.1

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