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SNP ID:
rs146562217
Gene
INSM2 RALGAPA1
Gene Name
INSM transcriptional repressor 2
Set Membership:
-
Chromosome Location:
Chr.14: 35539573 - 35539573 on Build GRCh38
Polymorphism:
C/T, Transition substitution
Context Sequence [VIC/FAM]:

TTTATTGGCTGAGCCAGAGGAACGA[C/T]GCAGCTTCATGGACATGCGGCTTTT

Assay ID C_163144269_10
Size
Availability Made To Order
Catalog # 4351379
Price (USD) 442.00
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Online offer (USD):407.65
407.65
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Genomic Map

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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 614027 MIM: 608884

Literature Links:

 INSM2 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
T (0.00)
(1.00)
Caucasian - Not Available CEPH (CEU) - Not Available
EAS
T (0.00)
(1.00)
African American - Not Available YRI (Yoruba) - Not Available
SAS
T (0.01)
(0.99)
Chinese - Not Available CHB (Han Chinese) - Not Available
AFR
T (0.00)
(1.00)
Japanese - Not Available JPT (Japanese) - Not Available
EUR
T (0.00)
(1.00)
AMR
T (0.00)
(1.00)
INSM2 - INSM transcriptional repressor 2
There are no transcripts associated with this gene.
RALGAPA1 - Ral GTPase activating protein catalytic alpha subunit 1
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001283043.1 5880 Intron NP_001269972.1
NM_001283044.1 5880 Intron NP_001269973.1
NM_014990.1 5880 Intron NP_055805.1
NM_194301.2 5880 Intron NP_919277.2
XM_005267491.3 5880 Intron XP_005267548.1
XM_005267492.3 5880 Intron XP_005267549.1
XM_005267493.3 5880 Intron XP_005267550.1
XM_005267498.4 5880 Missense Mutation CAT,CGT H,R 1316 XP_005267555.1
XM_006720098.2 5880 Intron XP_006720161.1
XM_006720099.2 5880 Intron XP_006720162.1
XM_006720100.3 5880 Intron XP_006720163.1
XM_006720101.2 5880 Intron XP_006720164.1
XM_006720102.3 5880 Intron XP_006720165.1
XM_006720103.2 5880 Intron XP_006720166.1
XM_006720104.3 5880 Intron XP_006720167.1
XM_011536615.2 5880 Intron XP_011534917.1
XM_011536616.2 5880 Intron XP_011534918.1
XM_017021141.1 5880 Intron XP_016876630.1
XM_017021142.1 5880 Intron XP_016876631.1
XM_017021143.1 5880 Intron XP_016876632.1
XM_017021144.1 5880 Intron XP_016876633.1
XM_017021145.1 5880 Intron XP_016876634.1
XM_017021146.1 5880 Missense Mutation CAT,CGT H,R 1825 XP_016876635.1
XM_017021147.1 5880 UTR 3 XP_016876636.1

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