Product Details

SNP ID

rs148761752

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:41621734 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCAGGACCCCAGTCACGATGCCAGC[A/G]ACGGCCCCCACAGGAAGGCCTGGGA

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CEACAM4 PubMed Links

Gene Details

Gene

CEACAM4

Gene Name

carcinoembryonic antigen related cell adhesion molecule 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001817.3	570	Intron			NP_001808.2
XM_006722977.3	570	Intron			XP_006723040.1
XM_011526343.1	570	Intron			XP_011524645.1
XM_011526345.2	570	Intron			XP_011524647.1
XM_011526348.2	570	Silent Mutation	GTC,GTT	V153V	XP_011524650.1
XM_011526349.2	570	Intron			XP_011524651.1
XM_011526350.2	570	Silent Mutation	GTC,GTT	V153V	XP_011524652.1
XM_011526352.1	570	Silent Mutation	GTC,GTT	V153V	XP_011524654.1
XM_011526354.1	570	Intron			XP_011524656.1
XM_011526357.2	570	Intron			XP_011524659.1
XM_017026199.1	570	Intron			XP_016881688.1
XM_017026200.1	570	Silent Mutation	GTC,GTT	V153V	XP_016881689.1
XM_017026201.1	570	Intron			XP_016881690.1
XM_017026202.1	570	Intron			XP_016881691.1
XM_017026203.1	570	Intron			XP_016881692.1
XM_017026204.1	570	Intron			XP_016881693.1
XM_017026205.1	570	Silent Mutation	GTC,GTT	V153V	XP_016881694.1
XM_017026206.1	570	Silent Mutation	GTC,GTT	V153V	XP_016881695.1
XM_017026207.1	570	Intron			XP_016881696.1
XM_017026208.1	570	Intron			XP_016881697.1
XM_017026209.1	570	Silent Mutation	GTC,GTT	V153V	XP_016881698.1
XM_017026210.1	570	Silent Mutation	GTC,GTT	V153V	XP_016881699.1
XM_017026211.1	570	Intron			XP_016881700.1
XM_017026212.1	570	Silent Mutation	GTC,GTT	V153V	XP_016881701.1
XM_017026213.1	570	Intron			XP_016881702.1

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