Product Details

SNP ID

rs61746548

Assay Type

Functionally tested

NCBI dbSNP Submissions

24

Location

Chr.1:3492708 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCCCACTGACAGGGTCGCAGTCAG[C/T]CCCACCCCCGCAGTCACAGTGCAGG

Phenotype

MIM: 604266

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MEGF6 PubMed Links

Gene Details

Gene

MEGF6

Gene Name

multiple EGF like domains 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001409.3	4309	Missense Mutation	ACT,GCT	T1483A	NP_001400.3
XM_006710406.3	4309	Missense Mutation	ACT,GCT	T1378A	XP_006710469.1
XM_011540885.1	4309	Missense Mutation	ACT,GCT	T1545A	XP_011539187.1
XM_011540886.1	4309	Missense Mutation	ACT,GCT	T1502A	XP_011539188.1
XM_011540887.2	4309	Missense Mutation	ACT,GCT	T1337A	XP_011539189.1
XM_011540888.2	4309	Intron			XP_011539190.1
XM_017000533.1	4309	Missense Mutation	ACT,GCT	T1501A	XP_016856022.1

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