Product Details
- SNP ID
-
rs142922966
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.20:47210799 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GTGTCCAGCCGAGACTCTTTCGGGA[A/G]GAGGCTCTTCGTGCTGGTACTGGTG
- Phenotype
-
MIM: 615713
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ZMYND8
PubMed Links
Gene Details
- Gene
- ZMYND8
- Gene Name
- zinc finger MYND-type containing 8
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001281769.1 |
4134 |
Intron |
|
|
NP_001268698.1 |
NM_001281771.2 |
4134 |
Missense Mutation |
CTC,TTC |
L1043F |
NP_001268700.1 |
NM_001281772.2 |
4134 |
Missense Mutation |
CTC,TTC |
L1175F |
NP_001268701.1 |
NM_001281773.2 |
4134 |
Missense Mutation |
CTC,TTC |
L1203F |
NP_001268702.1 |
NM_001281774.2 |
4134 |
Missense Mutation |
CTC,TTC |
L1157F |
NP_001268703.1 |
NM_001281775.2 |
4134 |
Missense Mutation |
CTC,TTC |
L1223F |
NP_001268704.1 |
NM_001281776.2 |
4134 |
Missense Mutation |
CTC,TTC |
L1096F |
NP_001268705.1 |
NM_001281777.2 |
4134 |
Missense Mutation |
CTC,TTC |
L1152F |
NP_001268706.1 |
NM_001281778.2 |
4134 |
Missense Mutation |
CTC,TTC |
L1170F |
NP_001268707.1 |
NM_001281779.2 |
4134 |
Missense Mutation |
CTC,TTC |
L909F |
NP_001268708.1 |
NM_001281780.2 |
4134 |
Missense Mutation |
CTC,TTC |
L881F |
NP_001268709.1 |
NM_001281781.2 |
4134 |
Missense Mutation |
CTC,TTC |
L1077F |
NP_001268710.1 |
NM_001281782.2 |
4134 |
Missense Mutation |
CTC,TTC |
L1125F |
NP_001268711.1 |
NM_001281783.2 |
4134 |
Missense Mutation |
CTC,TTC |
L1195F |
NP_001268712.1 |
NM_001281784.2 |
4134 |
Missense Mutation |
CTC,TTC |
L1123F |
NP_001268713.1 |
NM_012408.5 |
4134 |
Missense Mutation |
CTC,TTC |
L1149F |
NP_036540.3 |
NM_183047.3 |
4134 |
Missense Mutation |
CTC,TTC |
L1177F |
NP_898868.1 |
NM_183048.3 |
4134 |
Missense Mutation |
CTC,TTC |
L1124F |
NP_898869.1 |
XM_005260356.4 |
4134 |
Missense Mutation |
CTC,TTC |
L1230F |
XP_005260413.1 |
XM_005260358.2 |
4134 |
Missense Mutation |
CTC,TTC |
L1222F |
XP_005260415.1 |
XM_005260360.4 |
4134 |
Missense Mutation |
CTC,TTC |
L1203F |
XP_005260417.1 |
XM_005260362.2 |
4134 |
Missense Mutation |
CTC,TTC |
L1198F |
XP_005260419.1 |
XM_005260364.2 |
4134 |
Missense Mutation |
CTC,TTC |
L1178F |
XP_005260421.1 |
XM_005260366.2 |
4134 |
Missense Mutation |
CTC,TTC |
L1175F |
XP_005260423.1 |
XM_006723760.3 |
4134 |
Missense Mutation |
CTC,TTC |
L1222F |
XP_006723823.1 |
XM_006723762.3 |
4134 |
Missense Mutation |
CTC,TTC |
L1203F |
XP_006723825.1 |
XM_006723763.1 |
4134 |
Missense Mutation |
CTC,TTC |
L1197F |
XP_006723826.1 |
XM_006723766.1 |
4134 |
Missense Mutation |
CTC,TTC |
L1178F |
XP_006723829.1 |
XM_011528749.2 |
4134 |
Missense Mutation |
CTC,TTC |
L1228F |
XP_011527051.1 |
XM_011528751.1 |
4134 |
Missense Mutation |
CTC,TTC |
L1203F |
XP_011527053.1 |
XM_011528752.1 |
4134 |
Missense Mutation |
CTC,TTC |
L1156F |
XP_011527054.1 |
XM_011528753.1 |
4134 |
Missense Mutation |
CTC,TTC |
L1178F |
XP_011527055.1 |
XM_011528754.1 |
4134 |
Missense Mutation |
CTC,TTC |
L1178F |
XP_011527056.1 |
XM_017027760.1 |
4134 |
Silent Mutation |
TCC,TCT |
S1172S |
XP_016883249.1 |
XM_017027761.1 |
4134 |
Missense Mutation |
CTC,TTC |
L1203F |
XP_016883250.1 |
XM_017027762.1 |
4134 |
Missense Mutation |
CTC,TTC |
L1203F |
XP_016883251.1 |
XM_017027763.1 |
4134 |
Missense Mutation |
CTC,TTC |
L1194F |
XP_016883252.1 |
XM_017027764.1 |
4134 |
Silent Mutation |
TCC,TCT |
S1152S |
XP_016883253.1 |
XM_017027765.1 |
4134 |
Silent Mutation |
TCC,TCT |
S1147S |
XP_016883254.1 |
XM_017027766.1 |
4134 |
Missense Mutation |
CTC,TTC |
L1178F |
XP_016883255.1 |
XM_017027767.1 |
4134 |
Missense Mutation |
CTC,TTC |
L1175F |
XP_016883256.1 |
XM_017027768.1 |
4134 |
Missense Mutation |
CTC,TTC |
L1175F |
XP_016883257.1 |
XM_017027769.1 |
4134 |
Silent Mutation |
TCC,TCT |
S1127S |
XP_016883258.1 |
XM_017027770.1 |
4134 |
Missense Mutation |
CTC,TTC |
L1150F |
XP_016883259.1 |
XM_017027771.1 |
4134 |
Missense Mutation |
CTC,TTC |
L1150F |
XP_016883260.1 |
XM_017027772.1 |
4134 |
Missense Mutation |
CTC,TTC |
L1150F |
XP_016883261.1 |
XM_017027773.1 |
4134 |
Silent Mutation |
TCC,TCT |
S1101S |
XP_016883262.1 |
XM_017027774.1 |
4134 |
Missense Mutation |
CTC,TTC |
L1135F |
XP_016883263.1 |
XM_017027775.1 |
4134 |
Missense Mutation |
CTC,TTC |
L1132F |
XP_016883264.1 |
XM_017027776.1 |
4134 |
Silent Mutation |
TCC,TCT |
S1080S |
XP_016883265.1 |
XM_017027777.1 |
4134 |
Missense Mutation |
CTC,TTC |
L1107F |
XP_016883266.1 |
XM_017027778.1 |
4134 |
Intron |
|
|
XP_016883267.1 |
XM_017027779.1 |
4134 |
Missense Mutation |
CTC,TTC |
L906F |
XP_016883268.1 |
XM_017027780.1 |
4134 |
Missense Mutation |
CTC,TTC |
L898F |
XP_016883269.1 |
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