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See other FAM117A GT Assays ›
SNP ID:
rs8186
Gene
FAM117A SLC35B1
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.17: 49701431 - 49701431 on Build GRCh38
Polymorphism:
C/T, Transition substitution
Context Sequence [VIC/FAM]:

TGTTTGAGATAATAACTTAAATATT[C/T]TTGATGTGGAGGTAGTCTCTCTCTT

Assay ID C___7476482_10
Size
재고 정보 주문접수 후 제작
Catalog # 4351379
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Assay 상세 정보



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 610790

Literature Links:

 FAM117A PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
A (0.09)
(0.91)
Caucasian - Not Available CEPH (CEU)
A (0.07)
(0.93)
EAS
A (0.06)
(0.94)
African American - Not Available YRI (Yoruba)
A (0.13)
(0.87)
SAS
A (0.09)
(0.91)
Chinese - Not Available JPT (Japanese)
A (0.04)
(0.96)
AFR
A (0.13)
(0.87)
Japanese - Not Available CHB (Han Chinese)
A (0.07)
(0.93)
EUR
A (0.06)
(0.94)
AMR
A (0.11)
(0.89)
FAM117A - family with sequence similarity 117 member A
There are no transcripts associated with this gene.
SLC35B1 - solute carrier family 35 member B1
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001278784.1 999 UTR 3 NP_001265713.1
NM_005827.2 999 UTR 3 NP_005818.2
XM_005256929.3 999 UTR 3 XP_005256986.1
XM_006721632.3 999 UTR 3 XP_006721695.1
XM_011524179.2 999 UTR 3 XP_011522481.1
XM_011524180.2 999 UTR 3 XP_011522482.1

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추가 정보


Set Membership:

 HapMap

Panther Classification:

Molecular Function -

secondary carrier transporter

Gene Ontology Categories:

Function(s) Process(es)


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