Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCTTCTTGGCAAAGAACAGATGTA[C/T]CTCCTCAGTCTCCTTGTTGTGAAGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 300429 | ||||||||||||||||||||
Literature Links: |
ARHGEF9 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 |
ARHGEF9 - Cdc42 guanine nucleotide exchange factor 9 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001173479.1 | 2132 | Missense Mutation | ATA,GTA | I,V 349 | NP_001166950.1 | |
NM_001173480.1 | 2132 | Missense Mutation | ATA,GTA | I,V 300 | NP_001166951.1 | |
NM_015185.2 | 2132 | Missense Mutation | ATA,GTA | I,V 402 | NP_056000.1 | |
XM_005262249.2 | 2132 | Missense Mutation | ATA,GTA | I,V 409 | XP_005262306.1 | |
XM_005262250.3 | 2132 | Missense Mutation | ATA,GTA | I,V 381 | XP_005262307.1 | |
XM_005262251.1 | 2132 | Missense Mutation | ATA,GTA | I,V 381 | XP_005262308.1 | |
XM_005262252.1 | 2132 | Missense Mutation | ATA,GTA | I,V 381 | XP_005262309.1 | |
XM_011530890.1 | 2132 | Missense Mutation | ATA,GTA | I,V 402 | XP_011529192.1 | |
XM_011530892.1 | 2132 | Missense Mutation | ATA,GTA | I,V 342 | XP_011529194.1 | |
XM_017029363.1 | 2132 | Missense Mutation | ATA,GTA | I,V 407 | XP_016884852.1 | |
XM_017029364.1 | 2132 | Missense Mutation | ATA,GTA | I,V 407 | XP_016884853.1 | |
XM_017029365.1 | 2132 | Missense Mutation | ATA,GTA | I,V 402 | XP_016884854.1 | |
XM_017029366.1 | 2132 | Missense Mutation | ATA,GTA | I,V 402 | XP_016884855.1 | |
XM_017029367.1 | 2132 | Missense Mutation | ATA,GTA | I,V 381 | XP_016884856.1 | |
XM_017029368.1 | 2132 | Missense Mutation | ATA,GTA | I,V 381 | XP_016884857.1 | |
XM_017029369.1 | 2132 | Missense Mutation | ATA,GTA | I,V 365 | XP_016884858.1 | |
XM_017029370.1 | 2132 | Missense Mutation | ATA,GTA | I,V 358 | XP_016884859.1 | |
XM_017029371.1 | 2132 | Missense Mutation | ATA,GTA | I,V 337 | XP_016884860.1 | |
XM_017029372.1 | 2132 | Missense Mutation | ATA,GTA | I,V 337 | XP_016884861.1 | |
XM_017029373.1 | 2132 | Missense Mutation | ATA,GTA | I,V 300 | XP_016884862.1 | |
XM_017029374.1 | 2132 | Missense Mutation | ATA,GTA | I,V 298 | XP_016884863.1 | |
XM_017029375.1 | 2132 | Intron | XP_016884864.1 | |||
XM_017029376.1 | 2132 | Intron | XP_016884865.1 | |||
XM_017029377.1 | 2132 | Intron | XP_016884866.1 | |||
XM_017029378.1 | 2132 | UTR 3 | XP_016884867.1 | |||
XM_017029379.1 | 2132 | Intron | XP_016884868.1 | |||
XM_017029380.1 | 2132 | Intron | XP_016884869.1 |