Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCTGATCTTCCTCCTCCTCGGCCC[A/G]CCCAGAGCCTGGAGACAGCAGTTCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
3 submissions
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Phenotype: |
MIM: 614264 MIM: 609607 | ||||||||||||||||||||
Literature Links: |
ARHGAP30 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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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 |
ARHGAP30 - Rho GTPase activating protein 30 | ||||||
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There are no transcripts associated with this gene. |
NECTIN4 - nectin cell adhesion molecule 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_030916.2 | 1594 | Missense Mutation | CGG,TGG | R,W 467 | NP_112178.2 | |
XM_005245508.3 | 1594 | Missense Mutation | CGG,TGG | R,W 442 | XP_005245565.1 | |
XM_011510021.2 | 1594 | Missense Mutation | CGG,TGG | R,W 468 | XP_011508323.1 | |
XM_011510022.2 | 1594 | Missense Mutation | CGG,TGG | R,W 443 | XP_011508324.1 | |
XM_011510023.1 | 1594 | UTR 3 | XP_011508325.1 |