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See other ABCC4 GT Assays ›
SNP ID:
rs997777
Gene
ABCC4
Gene Name
Set Membership:
> HapMap > Validated
Chromosome Location:
Chr.13: 95141200 - 95141200 on Build GRCh38
Polymorphism:
A/T, Transversion substitution
Context Sequence [VIC/FAM]:

GAAAGGAGTAAAAGAGCTTTAATCC[A/T]CTGACATTACAAGTCGGAGGCAAAG

Assay ID C___7466543_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
Online offer:
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 605250

Literature Links:

 ABCC4 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
A (0.46)
(0.54)
Caucasian
A (0.36)
(0.64)
CEPH (CEU)
A (0.31)
(0.69)
EAS
A (0.38)
(0.62)
African American
T (0.21)
(0.79)
YRI (Yoruba)
T (0.19)
(0.81)
SAS
A (0.34)
(0.66)
Chinese - Not Available JPT (Japanese)
A (0.42)
(0.58)
AFR
T (0.22)
(0.78)
Japanese - Not Available CHB (Han Chinese)
A (0.36)
(0.64)
EUR
A (0.30)
(0.70)
AMR
A (0.38)
(0.62)
ABCC4 - ATP binding cassette subfamily C member 4
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001105515.2 Intron NP_001098985.1
NM_001301829.1 Intron NP_001288758.1
NM_001301830.1 Intron NP_001288759.1
NM_005845.4 Intron NP_005836.2
XM_005254025.2 Intron XP_005254082.1
XM_017020319.1 Intron XP_016875808.1
XM_017020320.1 Intron XP_016875809.1
XM_017020321.1 Intron XP_016875810.1
XM_017020322.1 Intron XP_016875811.1

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