Product Details

SNP ID

rs147510728

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:37126925 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATCCTTCTCAACCTTGTGGGATGTG[A/G]AAACTCTGTTACTGAAGGTTAGTAT

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ZCCHC7 PubMed Links

Gene Details

Gene

ZCCHC7

Gene Name

zinc finger CCHC-type containing 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001289119.1	766	Missense Mutation	GAA,GGA	E198G	NP_001276048.1
NM_001289120.1	766	Missense Mutation	GAA,GGA	E198G	NP_001276049.1
NM_001289121.1	766	Missense Mutation	GAA,GGA	E198G	NP_001276050.1
NM_032226.2	766	Missense Mutation	GAA,GGA	E198G	NP_115602.2
XM_005251608.4	766	Missense Mutation	GAA,GGA	E198G	XP_005251665.1
XM_005251612.2	766	Missense Mutation	GAA,GGA	E198G	XP_005251669.1
XM_011518050.1	766	Missense Mutation	GAA,GGA	E198G	XP_011516352.1
XM_011518051.2	766	Intron			XP_011516353.1
XM_017015197.1	766	Missense Mutation	GAA,GGA	E198G	XP_016870686.1
XM_017015198.1	766	Missense Mutation	GAA,GGA	E198G	XP_016870687.1
XM_017015199.1	766	Missense Mutation	AAA,GAA	K15E	XP_016870688.1
XM_017015200.1	766	Missense Mutation	AAA,GAA	K15E	XP_016870689.1
XM_017015201.1	766	Intron			XP_016870690.1

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