Product Details
- SNP ID
-
rs141420000
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:99486896 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGAATTCACTTTTTAGAGAATCCTT[C/T]TGAGTGTAAGGTCTGTGGGCAAGCC
- Phenotype
-
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ZNF394
PubMed Links
Gene Details
- Gene
- ZNF394
- Gene Name
- zinc finger protein 394
- Gene
- ZNF789
- Gene Name
- zinc finger protein 789
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001013258.1 |
860 |
Intron |
|
|
NP_001013276.1 |
NM_213603.2 |
860 |
Missense Mutation |
TCT,TTT |
S229F |
NP_998768.2 |
XM_011516067.2 |
860 |
Missense Mutation |
TCT,TTT |
S222F |
XP_011514369.1 |
XM_011516070.2 |
860 |
Missense Mutation |
TCT,TTT |
S212F |
XP_011514372.1 |
XM_011516073.2 |
860 |
Missense Mutation |
TCT,TTT |
S134F |
XP_011514375.1 |
XM_017012018.1 |
860 |
Missense Mutation |
TCT,TTT |
S229F |
XP_016867507.1 |
XM_017012019.1 |
860 |
Missense Mutation |
TCT,TTT |
S212F |
XP_016867508.1 |
XM_017012020.1 |
860 |
Missense Mutation |
TCT,TTT |
S212F |
XP_016867509.1 |
XM_017012021.1 |
860 |
Missense Mutation |
TCT,TTT |
S212F |
XP_016867510.1 |
XM_017012022.1 |
860 |
Missense Mutation |
TCT,TTT |
S212F |
XP_016867511.1 |
XM_017012023.1 |
860 |
Missense Mutation |
TCT,TTT |
S191F |
XP_016867512.1 |
XM_017012024.1 |
860 |
Missense Mutation |
TCT,TTT |
S171F |
XP_016867513.1 |
XM_017012025.1 |
860 |
Missense Mutation |
TCT,TTT |
S134F |
XP_016867514.1 |
XM_017012026.1 |
860 |
Missense Mutation |
TCT,TTT |
S134F |
XP_016867515.1 |
XM_017012027.1 |
860 |
Missense Mutation |
TCT,TTT |
S134F |
XP_016867516.1 |
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