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See other MGAT4C GT Assays ›
SNP ID:
rs981142
Gene
MGAT4C
Gene Name
Set Membership:
> HapMap > Validated
Chromosome Location:
Chr.12: 86704278 - 86704278 on Build GRCh38
Polymorphism:
G/T, Transversion substitution
Context Sequence [VIC/FAM]:

CCTAATTTAAGCTATGGGTCAGCCC[G/T]TTGGCTATGCTTGGATAGAGAATGA

Assay ID C___2774944_10
Size
Availability Made To Order
Catalog # 4351379
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 607385

Literature Links:

 MGAT4C PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
C (0.21)
(0.79)
Caucasian
G (0.03)
(0.97)
CEPH (CEU)
C (0.07)
(0.93)
EAS
C (0.28)
(0.72)
African American
G (0.27)
(0.73)
YRI (Yoruba)
C (0.35)
(0.65)
SAS
C (0.12)
(0.88)
Chinese - Not Available JPT (Japanese)
C (0.24)
(0.76)
AFR
C (0.36)
(0.64)
Japanese - Not Available CHB (Han Chinese)
C (0.24)
(0.76)
EUR
C (0.10)
(0.90)
AMR
C (0.14)
(0.86)
MGAT4C - MGAT4 family member C
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_013244.3 Intron NP_037376.2
XM_005268776.4 Intron XP_005268833.1
XM_005268779.3 Intron XP_005268836.1
XM_011538150.2 Intron XP_011536452.1
XM_011538151.2 Intron XP_011536453.1
XM_011538156.2 Intron XP_011536458.1
XM_011538157.2 Intron XP_011536459.1
XM_017019143.1 Intron XP_016874632.1
XM_017019144.1 Intron XP_016874633.1
XM_017019145.1 Intron XP_016874634.1
XM_017019146.1 Intron XP_016874635.1
XM_017019147.1 Intron XP_016874636.1
XM_017019148.1 Intron XP_016874637.1
XM_017019149.1 Intron XP_016874638.1
XM_017019150.1 Intron XP_016874639.1

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More Information


Set Membership:

 HapMap Validated

Panther Classification:

Molecular Function -

transferase

Gene Ontology Categories:

Function(s) Process(es)


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