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See other PHTF2 GT Assays ›
SNP ID:
rs7953
Gene
PHTF2 TMEM60
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.7: 77794257 - 77794257 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

TAGTATCAAATATCCAGACTGGAAT[A/G]AATATGAGGAACCAGTTCCAAGGTG

Assay ID C___8889630_30
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: 616785

Literature Links:

 PHTF2 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
C (0.43)
(0.57)
Caucasian - Not Available CEPH (CEU)
C (0.49)
(0.51)
EAS
T (0.32)
(0.68)
African American - Not Available YRI (Yoruba)
C (0.12)
(0.88)
SAS
C (0.43)
(0.57)
Chinese - Not Available JPT (Japanese)
T (0.36)
(0.64)
AFR
C (0.14)
(0.86)
Japanese - Not Available CHB (Han Chinese)
T (0.26)
(0.74)
EUR
C (0.49)
(0.51)
AMR
T (0.44)
(0.56)
PHTF2 - putative homeodomain transcription factor 2
There are no transcripts associated with this gene.
TMEM60 - transmembrane protein 60
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_032936.3 344 Silent Mutation TTC,TTT F,F 39 NP_116325.1

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More Information


Set Membership:

 HapMap

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