Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATGAACAGCAACTTCTGGCTGTCGG[C/G]AAACTCCTTCCCTTCCTGAAGGAAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 602663 MIM: 602206 | ||||||||||||||||||||
Literature Links: |
PRLH 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 |
PRLH - prolactin releasing hormone | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
RAB17 - RAB17, member RAS oncogene family | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022449.3 | 997 | Missense Mutation | CCC,GCC | P,A 151 | NP_071894.1 | |
XM_006712689.1 | 997 | Missense Mutation | CCC,GCC | P,A 129 | XP_006712752.1 | |
XM_017004693.1 | 997 | Intron | XP_016860182.1 | |||
XM_017004694.1 | 997 | Intron | XP_016860183.1 |