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CAGTGTGAACTCTCCGATGTAGTGC[A/G]AGGCATGAGTTGCGACTGAAACTTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 600398 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF160 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
ZNF160 - zinc finger protein 160 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
ZNF415 - zinc finger protein 415 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001136038.2 | 1547 | Silent Mutation | CTC,CTT | L,L 287 | NP_001129510.2 | |
NM_001164309.1 | 1547 | Silent Mutation | CTC,CTT | L,L 287 | NP_001157781.1 | |
NM_018355.3 | 1547 | Silent Mutation | CTC,CTT | L,L 287 | NP_060825.2 | |
XM_006723267.1 | 1547 | Silent Mutation | CTC,CTT | L,L 364 | XP_006723330.1 | |
XM_006723268.1 | 1547 | Silent Mutation | CTC,CTT | L,L 333 | XP_006723331.1 | |
XM_006723272.2 | 1547 | Silent Mutation | CTC,CTT | L,L 299 | XP_006723335.1 | |
XM_006723273.2 | 1547 | Silent Mutation | CTC,CTT | L,L 299 | XP_006723336.1 | |
XM_006723274.2 | 1547 | Silent Mutation | CTC,CTT | L,L 299 | XP_006723337.1 | |
XM_006723277.2 | 1547 | Silent Mutation | CTC,CTT | L,L 274 | XP_006723340.1 | |
XM_006723279.1 | 1547 | Silent Mutation | CTC,CTT | L,L 274 | XP_006723342.1 | |
XM_006723280.2 | 1547 | Silent Mutation | CTC,CTT | L,L 262 | XP_006723343.1 | |
XM_006723281.2 | 1547 | Silent Mutation | CTC,CTT | L,L 57 | XP_006723344.1 | |
XM_006723282.1 | 1547 | Silent Mutation | CTC,CTT | L,L 57 | XP_006723345.1 | |
XM_011527100.1 | 1547 | Silent Mutation | CTC,CTT | L,L 323 | XP_011525402.1 | |
XM_011527101.2 | 1547 | Silent Mutation | CTC,CTT | L,L 323 | XP_011525403.1 | |
XM_011527103.1 | 1547 | Silent Mutation | CTC,CTT | L,L 287 | XP_011525405.1 | |
XM_011527104.1 | 1547 | Silent Mutation | CTC,CTT | L,L 274 | XP_011525406.1 | |
XM_017026952.1 | 1547 | Silent Mutation | CTC,CTT | L,L 323 | XP_016882441.1 | |
XM_017026953.1 | 1547 | Silent Mutation | CTC,CTT | L,L 364 | XP_016882442.1 | |
XM_017026954.1 | 1547 | Silent Mutation | CTC,CTT | L,L 364 | XP_016882443.1 | |
XM_017026955.1 | 1547 | Silent Mutation | CTC,CTT | L,L 335 | XP_016882444.1 | |
XM_017026956.1 | 1547 | Silent Mutation | CTC,CTT | L,L 335 | XP_016882445.1 | |
XM_017026957.1 | 1547 | Silent Mutation | CTC,CTT | L,L 335 | XP_016882446.1 | |
XM_017026958.1 | 1547 | Silent Mutation | CTC,CTT | L,L 335 | XP_016882447.1 | |
XM_017026959.1 | 1547 | Silent Mutation | CTC,CTT | L,L 335 | XP_016882448.1 | |
XM_017026960.1 | 1547 | Silent Mutation | CTC,CTT | L,L 335 | XP_016882449.1 | |
XM_017026961.1 | 1547 | Silent Mutation | CTC,CTT | L,L 325 | XP_016882450.1 | |
XM_017026962.1 | 1547 | Silent Mutation | CTC,CTT | L,L 323 | XP_016882451.1 | |
XM_017026963.1 | 1547 | Silent Mutation | CTC,CTT | L,L 323 | XP_016882452.1 | |
XM_017026964.1 | 1547 | Silent Mutation | CTC,CTT | L,L 287 | XP_016882453.1 | |
XM_017026965.1 | 1547 | Silent Mutation | CTC,CTT | L,L 287 | XP_016882454.1 | |
XM_017026966.1 | 1547 | Silent Mutation | CTC,CTT | L,L 287 | XP_016882455.1 | |
XM_017026967.1 | 1547 | Silent Mutation | CTC,CTT | L,L 287 | XP_016882456.1 | |
XM_017026968.1 | 1547 | Silent Mutation | CTC,CTT | L,L 274 | XP_016882457.1 | |
XM_017026969.1 | 1547 | Silent Mutation | CTC,CTT | L,L 258 | XP_016882458.1 | |
XM_017026970.1 | 1547 | Silent Mutation | CTC,CTT | L,L 299 | XP_016882459.1 | |
XM_017026971.1 | 1547 | Silent Mutation | CTC,CTT | L,L 315 | XP_016882460.1 | |
XM_017026972.1 | 1547 | Silent Mutation | CTC,CTT | L,L 57 | XP_016882461.1 | |
XM_017026973.1 | 1547 | Silent Mutation | CTC,CTT | L,L 299 | XP_016882462.1 | |
XM_017026974.1 | 1547 | Silent Mutation | CTC,CTT | L,L 335 | XP_016882463.1 |