Product Details

SNP ID

rs200527749

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:121350548 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTTTGTATCCTTATTGTTCTTTAT[A/G]TGCTATTGGAACACAGTAATAATAT

Phenotype

MIM: 608618 MIM: 606267

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAM3C PubMed Links

Gene Details

Gene

FAM3C

Gene Name

family with sequence similarity 3 member C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001040020.1	937	Intron			NP_001035109.1
NM_014888.2	937	Intron			NP_055703.1
XM_011515736.2	937	Intron			XP_011514038.1
XM_011515737.2	937	Silent Mutation	CAC,CAT	H199H	XP_011514039.1

Gene

WNT16

Gene Name

Wnt family member 16

There are no transcripts associated with this gene.

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