Product Details

SNP ID

rs1634324

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:13044597 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCTGCAGAGGCTGGCACCGCGAAG[A/C]TCCTCCGAGGGCCTGGGTCCTCTGT

Phenotype

MIM: 300479

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

FAM9C PubMed Links

Gene Details

Gene

FAM9C

Gene Name

family with sequence similarity 9 member C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_174901.5	202	UTR 5			NP_777561.1
XM_005274460.2	202	Intron			XP_005274517.1
XM_017029321.1	202	Intron			XP_016884810.1

Gene

LOC105373133

Gene Name

uncharacterized LOC105373133

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_011545614.2	202	Missense Mutation	GAT,GCT	D15A	XP_011543916.1

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