Product Details

SNP ID

rs141420000

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:99486896 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAATTCACTTTTTAGAGAATCCTT[C/T]TGAGTGTAAGGTCTGTGGGCAAGCC

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ZNF394 PubMed Links

Gene Details

Gene

ZNF394

Gene Name

zinc finger protein 394

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032164.2	860	Intron			NP_115540.2
XM_017012710.1	860	UTR 3			XP_016868199.1
XM_017012711.1	860	Intron			XP_016868200.1

Gene

ZNF789

Gene Name

zinc finger protein 789

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001013258.1	860	Intron			NP_001013276.1
NM_213603.2	860	Missense Mutation	TCT,TTT	S229F	NP_998768.2
XM_011516067.2	860	Missense Mutation	TCT,TTT	S222F	XP_011514369.1
XM_011516070.2	860	Missense Mutation	TCT,TTT	S212F	XP_011514372.1
XM_011516073.2	860	Missense Mutation	TCT,TTT	S134F	XP_011514375.1
XM_017012018.1	860	Missense Mutation	TCT,TTT	S229F	XP_016867507.1
XM_017012019.1	860	Missense Mutation	TCT,TTT	S212F	XP_016867508.1
XM_017012020.1	860	Missense Mutation	TCT,TTT	S212F	XP_016867509.1
XM_017012021.1	860	Missense Mutation	TCT,TTT	S212F	XP_016867510.1
XM_017012022.1	860	Missense Mutation	TCT,TTT	S212F	XP_016867511.1
XM_017012023.1	860	Missense Mutation	TCT,TTT	S191F	XP_016867512.1
XM_017012024.1	860	Missense Mutation	TCT,TTT	S171F	XP_016867513.1
XM_017012025.1	860	Missense Mutation	TCT,TTT	S134F	XP_016867514.1
XM_017012026.1	860	Missense Mutation	TCT,TTT	S134F	XP_016867515.1
XM_017012027.1	860	Missense Mutation	TCT,TTT	S134F	XP_016867516.1

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