Product Details

SNP ID

rs7958826

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:85979493 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TAGGCATAACGTTTTCCCCAACATC[C/T]AGGGCTCCATGATGCAAAATATCAT

Phenotype

MIM: 607385

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MGAT4C PubMed Links

Gene Details

Gene

MGAT4C

Gene Name

MGAT4 family member C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_013244.3	1565	Silent Mutation	CTA,CTG	L411L	NP_037376.2
XM_005268776.4	1565	Silent Mutation	CTA,CTG	L440L	XP_005268833.1
XM_005268779.3	1565	Silent Mutation	CTA,CTG	L411L	XP_005268836.1
XM_011538150.2	1565	Silent Mutation	CTA,CTG	L449L	XP_011536452.1
XM_011538151.2	1565	Silent Mutation	CTA,CTG	L449L	XP_011536453.1
XM_011538156.2	1565	Silent Mutation	CTA,CTG	L411L	XP_011536458.1
XM_011538157.2	1565	Silent Mutation	CTA,CTG	L411L	XP_011536459.1
XM_017019143.1	1565	Silent Mutation	CTA,CTG	L460L	XP_016874632.1
XM_017019144.1	1565	Silent Mutation	CTA,CTG	L449L	XP_016874633.1
XM_017019145.1	1565	Silent Mutation	CTA,CTG	L440L	XP_016874634.1
XM_017019146.1	1565	Silent Mutation	CTA,CTG	L440L	XP_016874635.1
XM_017019147.1	1565	Silent Mutation	CTA,CTG	L440L	XP_016874636.1
XM_017019148.1	1565	Silent Mutation	CTA,CTG	L411L	XP_016874637.1
XM_017019149.1	1565	Silent Mutation	CTA,CTG	L411L	XP_016874638.1
XM_017019150.1	1565	Silent Mutation	CTA,CTG	L411L	XP_016874639.1

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