Product Details

SNP ID

rs142430931

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:10850548 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCAGCTGTCAGACCTCAGCGAGCC[C/T]GTGAACGTCTCCTTCCCAGGTAAGG

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

C19orf38 PubMed Links

Gene Details

Gene

C19orf38

Gene Name

chromosome 19 open reading frame 38

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001136482.1	746	Silent Mutation	CCC,CCT	P107P	NP_001129954.1
XM_005259846.4	746	Silent Mutation	CCC,CCT	P107P	XP_005259903.1
XM_005259847.4	746	Silent Mutation	CCC,CCT	P107P	XP_005259904.1

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