Product Details

SNP ID

rs180924502

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:38454226 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAGACGTGCTGGACACACTGGAGG[A/C]GCTGGGGTGAGTGCTTTTGGAGACG

Phenotype

MIM: 616142

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

FAM98B PubMed Links

Gene Details

Gene

FAM98B

Gene Name

family with sequence similarity 98 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173611.3	100	Missense Mutation	GAG,GCG	E22A	NP_775882.2

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