Product Details

SNP ID

rs112278435

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:47210839 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGTACTGGTGTTGTGATCGGAACG[C/T]GTCGATCCCCTCTTCTCATCACTGC

Phenotype

MIM: 615713

Polymorphism

C/T, 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	4094	Intron			NP_001268698.1
NM_001281771.2	4094	Silent Mutation	ACA,ACG	T1029T	NP_001268700.1
NM_001281772.2	4094	Silent Mutation	ACA,ACG	T1161T	NP_001268701.1
NM_001281773.2	4094	Silent Mutation	ACA,ACG	T1189T	NP_001268702.1
NM_001281774.2	4094	Silent Mutation	ACA,ACG	T1143T	NP_001268703.1
NM_001281775.2	4094	Silent Mutation	ACA,ACG	T1209T	NP_001268704.1
NM_001281776.2	4094	Silent Mutation	ACA,ACG	T1082T	NP_001268705.1
NM_001281777.2	4094	Silent Mutation	ACA,ACG	T1138T	NP_001268706.1
NM_001281778.2	4094	Silent Mutation	ACA,ACG	T1156T	NP_001268707.1
NM_001281779.2	4094	Silent Mutation	ACA,ACG	T895T	NP_001268708.1
NM_001281780.2	4094	Silent Mutation	ACA,ACG	T867T	NP_001268709.1
NM_001281781.2	4094	Silent Mutation	ACA,ACG	T1063T	NP_001268710.1
NM_001281782.2	4094	Silent Mutation	ACA,ACG	T1111T	NP_001268711.1
NM_001281783.2	4094	Silent Mutation	ACA,ACG	T1181T	NP_001268712.1
NM_001281784.2	4094	Silent Mutation	ACA,ACG	T1109T	NP_001268713.1
NM_012408.5	4094	Silent Mutation	ACA,ACG	T1135T	NP_036540.3
NM_183047.3	4094	Silent Mutation	ACA,ACG	T1163T	NP_898868.1
NM_183048.3	4094	Silent Mutation	ACA,ACG	T1110T	NP_898869.1
XM_005260356.4	4094	Silent Mutation	ACA,ACG	T1216T	XP_005260413.1
XM_005260358.2	4094	Silent Mutation	ACA,ACG	T1208T	XP_005260415.1
XM_005260360.4	4094	Silent Mutation	ACA,ACG	T1189T	XP_005260417.1
XM_005260362.2	4094	Silent Mutation	ACA,ACG	T1184T	XP_005260419.1
XM_005260364.2	4094	Silent Mutation	ACA,ACG	T1164T	XP_005260421.1
XM_005260366.2	4094	Silent Mutation	ACA,ACG	T1161T	XP_005260423.1
XM_006723760.3	4094	Silent Mutation	ACA,ACG	T1208T	XP_006723823.1
XM_006723762.3	4094	Silent Mutation	ACA,ACG	T1189T	XP_006723825.1
XM_006723763.1	4094	Silent Mutation	ACA,ACG	T1183T	XP_006723826.1
XM_006723766.1	4094	Silent Mutation	ACA,ACG	T1164T	XP_006723829.1
XM_011528749.2	4094	Silent Mutation	ACA,ACG	T1214T	XP_011527051.1
XM_011528751.1	4094	Silent Mutation	ACA,ACG	T1189T	XP_011527053.1
XM_011528752.1	4094	Silent Mutation	ACA,ACG	T1142T	XP_011527054.1
XM_011528753.1	4094	Silent Mutation	ACA,ACG	T1164T	XP_011527055.1
XM_011528754.1	4094	Silent Mutation	ACA,ACG	T1164T	XP_011527056.1
XM_017027760.1	4094	Missense Mutation	CAC,CGC	H1159R	XP_016883249.1
XM_017027761.1	4094	Silent Mutation	ACA,ACG	T1189T	XP_016883250.1
XM_017027762.1	4094	Silent Mutation	ACA,ACG	T1189T	XP_016883251.1
XM_017027763.1	4094	Silent Mutation	ACA,ACG	T1180T	XP_016883252.1
XM_017027764.1	4094	Missense Mutation	CAC,CGC	H1139R	XP_016883253.1
XM_017027765.1	4094	Missense Mutation	CAC,CGC	H1134R	XP_016883254.1
XM_017027766.1	4094	Silent Mutation	ACA,ACG	T1164T	XP_016883255.1
XM_017027767.1	4094	Silent Mutation	ACA,ACG	T1161T	XP_016883256.1
XM_017027768.1	4094	Silent Mutation	ACA,ACG	T1161T	XP_016883257.1
XM_017027769.1	4094	Missense Mutation	CAC,CGC	H1114R	XP_016883258.1
XM_017027770.1	4094	Silent Mutation	ACA,ACG	T1136T	XP_016883259.1
XM_017027771.1	4094	Silent Mutation	ACA,ACG	T1136T	XP_016883260.1
XM_017027772.1	4094	Silent Mutation	ACA,ACG	T1136T	XP_016883261.1
XM_017027773.1	4094	Missense Mutation	CAC,CGC	H1088R	XP_016883262.1
XM_017027774.1	4094	Silent Mutation	ACA,ACG	T1121T	XP_016883263.1
XM_017027775.1	4094	Silent Mutation	ACA,ACG	T1118T	XP_016883264.1
XM_017027776.1	4094	Missense Mutation	CAC,CGC	H1067R	XP_016883265.1
XM_017027777.1	4094	Silent Mutation	ACA,ACG	T1093T	XP_016883266.1
XM_017027778.1	4094	Intron			XP_016883267.1
XM_017027779.1	4094	Silent Mutation	ACA,ACG	T892T	XP_016883268.1
XM_017027780.1	4094	Silent Mutation	ACA,ACG	T884T	XP_016883269.1

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