Product Details

SNP ID

rs140904478

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:195747267 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGGACCACGAACGTCCCGACCCCC[A/G]GCAGCAAGAGGCCGCCCAGGGCCCC

Phenotype

MIM: 158372

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MUC4 PubMed Links

Gene Details

Gene

MUC4

Gene Name

mucin 4, cell surface associated

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001322468.1	22322	Missense Mutation			NP_001309397.1
NM_004532.5	22322	Missense Mutation	CCG,CTG	P1147L	NP_004523.3
NM_018406.6	22322	Intron			NP_060876.5
NM_138297.4	22322	Missense Mutation	CCG,CTG	P1096L	NP_612154.2

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