Product Details

SNP ID

rs142666003

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.18:74436566 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGAGTTGGCGAAGCTTCCAGAACA[C/T]GCTGGAGGCTGCTCTCCGGGTGTTC

Phenotype

MIM: 614544

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM69C PubMed Links

Gene Details

Gene

FAM69C

Gene Name

family with sequence similarity 69 member C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001044369.2	1250	Missense Mutation			NP_001037834.2
XM_011525816.2	1250	Missense Mutation			XP_011524118.1
XM_017025551.1	1250	Missense Mutation			XP_016881040.1

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