Product Details

SNP ID

rs11699901

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:44337201 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACCGTGGGCCTGGCAGGCCTGCTCT[G/T]CTGGGCTGGCCAGGCAGTGAACGCC

Phenotype

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

R3HDML PubMed Links

Gene Details

Gene

R3HDML

Gene Name

R3H domain containing like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_178491.3	44	Missense Mutation	TGC,TTC	C15F	NP_848586.1

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