Product Details

SNP ID

rs201142216

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:47210872 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCTCTTCTCATCACTGCTGCTCCA[A/G]CTGGATTTATTACTCCGGGAATGGT

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	4061	Intron			NP_001268698.1
NM_001281771.2	4061	Silent Mutation	AGC,AGT	S1018S	NP_001268700.1
NM_001281772.2	4061	Silent Mutation	AGC,AGT	S1150S	NP_001268701.1
NM_001281773.2	4061	Silent Mutation	AGC,AGT	S1178S	NP_001268702.1
NM_001281774.2	4061	Silent Mutation	AGC,AGT	S1132S	NP_001268703.1
NM_001281775.2	4061	Silent Mutation	AGC,AGT	S1198S	NP_001268704.1
NM_001281776.2	4061	Silent Mutation	AGC,AGT	S1071S	NP_001268705.1
NM_001281777.2	4061	Silent Mutation	AGC,AGT	S1127S	NP_001268706.1
NM_001281778.2	4061	Silent Mutation	AGC,AGT	S1145S	NP_001268707.1
NM_001281779.2	4061	Silent Mutation	AGC,AGT	S884S	NP_001268708.1
NM_001281780.2	4061	Silent Mutation	AGC,AGT	S856S	NP_001268709.1
NM_001281781.2	4061	Silent Mutation	AGC,AGT	S1052S	NP_001268710.1
NM_001281782.2	4061	Silent Mutation	AGC,AGT	S1100S	NP_001268711.1
NM_001281783.2	4061	Silent Mutation	AGC,AGT	S1170S	NP_001268712.1
NM_001281784.2	4061	Silent Mutation	AGC,AGT	S1098S	NP_001268713.1
NM_012408.5	4061	Silent Mutation	AGC,AGT	S1124S	NP_036540.3
NM_183047.3	4061	Silent Mutation	AGC,AGT	S1152S	NP_898868.1
NM_183048.3	4061	Silent Mutation	AGC,AGT	S1099S	NP_898869.1
XM_005260356.4	4061	Silent Mutation	AGC,AGT	S1205S	XP_005260413.1
XM_005260358.2	4061	Silent Mutation	AGC,AGT	S1197S	XP_005260415.1
XM_005260360.4	4061	Silent Mutation	AGC,AGT	S1178S	XP_005260417.1
XM_005260362.2	4061	Silent Mutation	AGC,AGT	S1173S	XP_005260419.1
XM_005260364.2	4061	Silent Mutation	AGC,AGT	S1153S	XP_005260421.1
XM_005260366.2	4061	Silent Mutation	AGC,AGT	S1150S	XP_005260423.1
XM_006723760.3	4061	Silent Mutation	AGC,AGT	S1197S	XP_006723823.1
XM_006723762.3	4061	Silent Mutation	AGC,AGT	S1178S	XP_006723825.1
XM_006723763.1	4061	Silent Mutation	AGC,AGT	S1172S	XP_006723826.1
XM_006723766.1	4061	Silent Mutation	AGC,AGT	S1153S	XP_006723829.1
XM_011528749.2	4061	Silent Mutation	AGC,AGT	S1203S	XP_011527051.1
XM_011528751.1	4061	Silent Mutation	AGC,AGT	S1178S	XP_011527053.1
XM_011528752.1	4061	Silent Mutation	AGC,AGT	S1131S	XP_011527054.1
XM_011528753.1	4061	Silent Mutation	AGC,AGT	S1153S	XP_011527055.1
XM_011528754.1	4061	Silent Mutation	AGC,AGT	S1153S	XP_011527056.1
XM_017027760.1	4061	Missense Mutation	GCT,GTT	A1148V	XP_016883249.1
XM_017027761.1	4061	Silent Mutation	AGC,AGT	S1178S	XP_016883250.1
XM_017027762.1	4061	Silent Mutation	AGC,AGT	S1178S	XP_016883251.1
XM_017027763.1	4061	Silent Mutation	AGC,AGT	S1169S	XP_016883252.1
XM_017027764.1	4061	Missense Mutation	GCT,GTT	A1128V	XP_016883253.1
XM_017027765.1	4061	Missense Mutation	GCT,GTT	A1123V	XP_016883254.1
XM_017027766.1	4061	Silent Mutation	AGC,AGT	S1153S	XP_016883255.1
XM_017027767.1	4061	Silent Mutation	AGC,AGT	S1150S	XP_016883256.1
XM_017027768.1	4061	Silent Mutation	AGC,AGT	S1150S	XP_016883257.1
XM_017027769.1	4061	Missense Mutation	GCT,GTT	A1103V	XP_016883258.1
XM_017027770.1	4061	Silent Mutation	AGC,AGT	S1125S	XP_016883259.1
XM_017027771.1	4061	Silent Mutation	AGC,AGT	S1125S	XP_016883260.1
XM_017027772.1	4061	Silent Mutation	AGC,AGT	S1125S	XP_016883261.1
XM_017027773.1	4061	Missense Mutation	GCT,GTT	A1077V	XP_016883262.1
XM_017027774.1	4061	Silent Mutation	AGC,AGT	S1110S	XP_016883263.1
XM_017027775.1	4061	Silent Mutation	AGC,AGT	S1107S	XP_016883264.1
XM_017027776.1	4061	Missense Mutation	GCT,GTT	A1056V	XP_016883265.1
XM_017027777.1	4061	Silent Mutation	AGC,AGT	S1082S	XP_016883266.1
XM_017027778.1	4061	Intron			XP_016883267.1
XM_017027779.1	4061	Silent Mutation	AGC,AGT	S881S	XP_016883268.1
XM_017027780.1	4061	Silent Mutation	AGC,AGT	S873S	XP_016883269.1

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