Product Details

SNP ID

rs34013660

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:96877964 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTAGCCAGGTCCTTGAGCATGGTGC[A/G]GTGCATGGCCTGGGGGCTCTCCCGG

Phenotype

MIM: 604462

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAM178B PubMed Links

Gene Details

Gene

FAM178B

Gene Name

family with sequence similarity 178 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001122646.2	385	Missense Mutation	CGC,TGC	R645C	NP_001116118.2
NM_001172667.1	385	Missense Mutation	CGC,TGC	R104C	NP_001166138.1
NM_016490.4	385	Missense Mutation	CGC,TGC	R85C	NP_057574.2
XM_011511294.2	385	Missense Mutation	CGC,TGC	R609C	XP_011509596.1
XM_011511297.2	385	Intron			XP_011509599.1
XM_017004263.1	385	Missense Mutation	CGC,TGC	R688C	XP_016859752.1
XM_017004264.1	385	Missense Mutation	CGC,TGC	R675C	XP_016859753.1
XM_017004265.1	385	Intron			XP_016859754.1
XM_017004266.1	385	Missense Mutation	CGC,TGC	R111C	XP_016859755.1
XM_017004267.1	385	Missense Mutation	CGC,TGC	R110C	XP_016859756.1
XM_017004268.1	385	Missense Mutation	CGC,TGC	R85C	XP_016859757.1

Gene

SEMA4C

Gene Name

semaphorin 4C

There are no transcripts associated with this gene.

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