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SNP ID:
rs61804848
Gene
CRTC2 DENND4B MIR6737 SLC39A1
Gene Name
Set Membership:
-
Chromosome Location:
Chr.1: 153952604 - 153952604 on Build GRCh38
Polymorphism:
G/T, Transversion substitution
Context Sequence [VIC/FAM]:

CATCCCATGGCTTCAGCAAATGCTT[G/T]TCATCTAGCAAGTTCTCCTCAATAG

Assay ID C__88349720_10
Size
Availability Made To Order
Catalog # 4351379
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 1 submissions

Phenotype:

 MIM: 608972 MIM: 604740

Literature Links:

 CRTC2 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global - Not Available Caucasian - Not Available CEPH (CEU) - Not Available
EAS - Not Available African American - Not Available YRI (Yoruba) - Not Available
SAS - Not Available Chinese - Not Available CHB (Han Chinese) - Not Available
AFR - Not Available Japanese - Not Available JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available
CRTC2 - CREB regulated transcription coactivator 2
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_181715.2 828 Missense Mutation GAA,GAC E,D 223 NP_859066.1
XM_005244946.1 828 Missense Mutation GAA,GAC E,D 228 XP_005245003.1
XM_005244949.2 828 Missense Mutation GAA,GAC E,D 115 XP_005245006.1
XM_017000575.1 828 Missense Mutation GAA,GAC E,D 150 XP_016856064.1
XM_017000576.1 828 Missense Mutation GAA,GAC E,D 145 XP_016856065.1
XM_017000577.1 828 Missense Mutation GAA,GAC E,D 127 XP_016856066.1
XM_017000578.1 828 Missense Mutation GAA,GAC E,D 122 XP_016856067.1
XM_017000579.1 828 Missense Mutation GAA,GAC E,D 17 XP_016856068.1
DENND4B - DENN domain containing 4B
There are no transcripts associated with this gene.
MIR6737 - microRNA 6737
There are no transcripts associated with this gene.
SLC39A1 - solute carrier family 39 member 1
There are no transcripts associated with this gene.

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