Product Details

SNP ID

rs35690935

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:737954 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCGAACCAGAGACCAGAACCGTGC[A/G]CCCTCCCTCACTCTTCGAAACTTCC

Phenotype

MIM: 611627 MIM: 606969

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAM57A PubMed Links

Gene Details

Gene

FAM57A

Gene Name

family with sequence similarity 57 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001318006.1	417	Silent Mutation	GCA,GCG	A105A	NP_001304935.1
NM_001318007.1	417	Intron			NP_001304936.1
NM_001318008.1	417	Intron			NP_001304937.1
NM_024792.2	417	Silent Mutation	GCA,GCG	A105A	NP_079068.1

Gene

GEMIN4

Gene Name

gem nuclear organelle associated protein 4

There are no transcripts associated with this gene.

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