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See other ATP5C1 GT Assays ›
SNP ID:
rs1244422
Gene
ATP5C1 KIN
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.10: 7796969 - 7796969 on Build GRCh38
Polymorphism:
C/T, Transition substitution
Context Sequence [VIC/FAM]:

GCGCTCATTATTCTGCCTTGCACTT[C/T]AGAAAAATATGTCAATAAATTCACA

Assay ID C___2735542_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: 108729 MIM: 601720

Literature Links:

 ATP5C1 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
T (0.46)
(0.54)
Caucasian - Not Available CEPH (CEU)
T (0.43)
(0.57)
EAS
T (0.33)
(0.67)
African American - Not Available YRI (Yoruba)
C (0.49)
(0.51)
SAS
C (0.39)
(0.61)
Chinese - Not Available JPT (Japanese)
T (0.34)
(0.66)
AFR
T (0.46)
(0.54)
Japanese - Not Available CHB (Han Chinese)
T (0.33)
(0.67)
EUR
T (0.41)
(0.59)
AMR
C (0.49)
(0.51)
ATP5C1 - ATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide 1
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001001973.2 Intron NP_001001973.1
NM_001320886.1 Intron NP_001307815.1
NM_005174.3 Intron NP_005165.1
XM_017016290.1 Intron XP_016871779.1
KIN - Kin17 DNA and RNA binding protein
There are no transcripts associated with this gene.

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