Product Details

SNP ID

rs200823619

Assay Type

Functionally tested

NCBI dbSNP Submissions

8

Location

Chr.1:248850497 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCAGGGAAGCCTTCTGGCGGCAGG[G/T]AAACCCGCATATCTCACACCTGGAG

Phenotype

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

ZNF672 PubMed Links

Gene Details

Gene

ZNF672

Gene Name

zinc finger protein 672

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024836.2	1484	Intron			NP_079112.1
XM_005270336.1	1484	Intron			XP_005270393.1

Gene

ZNF692

Gene Name

zinc finger protein 692

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001136036.2	1484	Missense Mutation	ACC,CCC	T430P	NP_001129508.1
NM_001193328.1	1484	Missense Mutation	ACC,CCC	T380P	NP_001180257.1
NM_017865.3	1484	Missense Mutation	ACC,CCC	T425P	NP_060335.2
XM_011544220.1	1484	Missense Mutation	ACC,CCC	T576P	XP_011542522.1
XM_011544221.1	1484	Missense Mutation	ACC,CCC	T575P	XP_011542523.1
XM_011544222.1	1484	Missense Mutation	ACC,CCC	T425P	XP_011542524.1
XM_011544223.2	1484	Missense Mutation	ACC,CCC	T531P	XP_011542525.1
XM_011544227.1	1484	Missense Mutation	ACC,CCC	T398P	XP_011542529.1
XM_017001698.1	1484	Missense Mutation	ACC,CCC	T424P	XP_016857187.1
XM_017001699.1	1484	Missense Mutation	ACC,CCC	T550P	XP_016857188.1
XM_017001700.1	1484	Missense Mutation	ACC,CCC	T399P	XP_016857189.1
XM_017001701.1	1484	Missense Mutation	ACC,CCC	T424P	XP_016857190.1
XM_017001702.1	1484	Missense Mutation	ACC,CCC	T399P	XP_016857191.1
XM_017001703.1	1484	Missense Mutation	ACC,CCC	T221P	XP_016857192.1
XM_017001704.1	1484	Missense Mutation	ACC,CCC	T221P	XP_016857193.1
XM_017001705.1	1484	Missense Mutation	ACC,CCC	T221P	XP_016857194.1

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