Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTTCCCTCCAATCTCATTTCTCTGG[C/T]GTTTGGAAGGATTTGGGCTGTGGTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602187 | ||||||||||||||||||||
Literature Links: |
ZNF195 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 |
ZNF195 - zinc finger protein 195 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130519.2 | 1718 | Missense Mutation | CAC,CGC | H,R 377 | NP_001123991.1 | |
NM_001130520.2 | 1718 | Missense Mutation | CAC,CGC | H,R 400 | NP_001123992.1 | |
NM_001242841.1 | 1718 | Missense Mutation | CAC,CGC | H,R 381 | NP_001229770.1 | |
NM_001242842.1 | 1718 | Missense Mutation | CAC,CGC | H,R 355 | NP_001229771.1 | |
NM_001242843.1 | 1718 | Missense Mutation | CAC,CGC | H,R 332 | NP_001229772.1 | |
NM_001256823.1 | 1718 | UTR 3 | NP_001243752.1 | |||
NM_001256824.1 | 1718 | Missense Mutation | CAC,CGC | H,R 363 | NP_001243753.1 | |
NM_001256825.1 | 1718 | Missense Mutation | CAC,CGC | H,R 332 | NP_001243754.1 | |
NM_007152.4 | 1718 | Missense Mutation | CAC,CGC | H,R 328 | NP_009083.2 | |
XM_006718306.1 | 1718 | Missense Mutation | CAC,CGC | H,R 343 | XP_006718369.1 | |
XM_011520350.2 | 1718 | Missense Mutation | CAC,CGC | H,R 404 | XP_011518652.1 | |
XM_011520351.2 | 1718 | Missense Mutation | CAC,CGC | H,R 404 | XP_011518653.1 | |
XM_011520352.2 | 1718 | Missense Mutation | CAC,CGC | H,R 366 | XP_011518654.1 | |
XM_011520354.2 | 1718 | Intron | XP_011518656.2 | |||
XM_017018260.1 | 1718 | Missense Mutation | CAC,CGC | H,R 415 | XP_016873749.1 | |
XM_017018261.1 | 1718 | Missense Mutation | CAC,CGC | H,R 404 | XP_016873750.1 | |
XM_017018262.1 | 1718 | Missense Mutation | CAC,CGC | H,R 392 | XP_016873751.1 | |
XM_017018263.1 | 1718 | Missense Mutation | CAC,CGC | H,R 381 | XP_016873752.1 | |
XM_017018264.1 | 1718 | Missense Mutation | CAC,CGC | H,R 260 | XP_016873753.1 | |
XM_017018265.1 | 1718 | Missense Mutation | CAC,CGC | H,R 301 | XP_016873754.1 | |
XM_017018266.1 | 1718 | Missense Mutation | CAC,CGC | H,R 301 | XP_016873755.1 | |
XM_017018267.1 | 1718 | Missense Mutation | CAC,CGC | H,R 324 | XP_016873756.1 |