Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGTTCAGCAACATAATCCAGAAAGC[A/G]GCGAGGAAGCTGTGACCCTGTTGGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 609601 | ||||||||||||||||||||
Literature Links: |
ZNF397 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 |
ZNF397 - zinc finger protein 397 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135178.2 | 508 | Missense Mutation | AGC,GGC | S,G 118 | NP_001128650.1 | |
NM_032347.2 | 508 | Missense Mutation | AGC,GGC | S,G 118 | NP_115723.1 | |
XM_006722558.2 | 508 | Missense Mutation | AGC,GGC | S,G 118 | XP_006722621.1 | |
XM_011526229.2 | 508 | Missense Mutation | AGC,GGC | S,G 118 | XP_011524531.1 | |
XM_011526230.2 | 508 | Missense Mutation | AGC,GGC | S,G 118 | XP_011524532.1 | |
XM_011526231.2 | 508 | Missense Mutation | AGC,GGC | S,G 118 | XP_011524533.1 | |
XM_017026042.1 | 508 | Missense Mutation | AGC,GGC | S,G 118 | XP_016881531.1 |
ZSCAN30 - zinc finger and SCAN domain containing 30 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |