Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATGGGTCAGGATTCCTGCCAGGTCC[A/C]CGATGTGTATCCAGGGGAAGAATTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 616162 | ||||||||||||||||||||
Literature Links: |
KHNYN 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 |
KHNYN - KH and NYN domain containing | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001290256.1 | 579 | UTR 3 | NP_001277185.1 | |||
NM_001290257.1 | 579 | UTR 3 | NP_001277186.1 | |||
NM_015299.2 | 579 | UTR 3 | NP_056114.1 | |||
XM_005267474.4 | 579 | UTR 3 | XP_005267531.1 | |||
XM_011536590.2 | 579 | UTR 3 | XP_011534892.1 | |||
XM_017021114.1 | 579 | Intron | XP_016876603.1 |
LOC101927045 - uncharacterized LOC101927045 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
SDR39U1 - short chain dehydrogenase/reductase family 39U member 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001290292.1 | 579 | Missense Mutation | GGG,GTG | G,V 114 | NP_001277221.1 | |
NM_001290293.2 | 579 | Missense Mutation | GGG,GTG | G,V 88 | NP_001277222.1 | |
NM_001308075.1 | 579 | Missense Mutation | GGG,GTG | G,V 114 | NP_001295004.1 | |
NM_020195.2 | 579 | Missense Mutation | GGG,GTG | G,V 196 | NP_064580.2 | |
XM_011536975.1 | 579 | Missense Mutation | GGG,GTG | G,V 219 | XP_011535277.1 | |
XM_011536976.1 | 579 | Missense Mutation | GGG,GTG | G,V 154 | XP_011535278.1 |