Product Details

SNP ID

rs202137114

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:45616474 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGCTTTGGTGCATTAACCACAGGAT[C/T]TGCCTCGTGCAAGTATCTCCTCCCT

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ZFAND4 PubMed Links

Gene Details

Gene

ZFAND4

Gene Name

zinc finger AN1-type containing 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001128324.2	2848	Missense Mutation	AAT,GAT	N716D	NP_001121796.1
NM_001282905.1	2848	Missense Mutation	AAT,GAT	N642D	NP_001269834.1
NM_001282906.1	2848	Missense Mutation	AAT,GAT	N642D	NP_001269835.1
NM_174890.3	2848	Missense Mutation	AAT,GAT	N716D	NP_777550.2
XM_005271842.2	2848	Missense Mutation	AAT,GAT	N617D	XP_005271899.1
XM_005271843.2	2848	Missense Mutation	AAT,GAT	N617D	XP_005271900.1
XM_005271844.3	2848	Missense Mutation	AAT,GAT	N598D	XP_005271901.1
XM_011540366.2	2848	Missense Mutation	AAT,GAT	N724D	XP_011538668.1
XM_011540368.1	2848	Missense Mutation	AAT,GAT	N544D	XP_011538670.1
XM_017016931.1	2848	Missense Mutation	AAT,GAT	N730D	XP_016872420.1
XM_017016932.1	2848	Missense Mutation	AAT,GAT	N722D	XP_016872421.1
XM_017016933.1	2848	Missense Mutation	AAT,GAT	N722D	XP_016872422.1
XM_017016934.1	2848	Missense Mutation	AAT,GAT	N722D	XP_016872423.1
XM_017016935.1	2848	Intron			XP_016872424.1
XM_017016936.1	2848	Missense Mutation	AAT,GAT	N674D	XP_016872425.1
XM_017016937.1	2848	Missense Mutation	AAT,GAT	N674D	XP_016872426.1
XM_017016938.1	2848	Missense Mutation	AAT,GAT	N668D	XP_016872427.1
XM_017016939.1	2848	Missense Mutation	AAT,GAT	N668D	XP_016872428.1
XM_017016940.1	2848	Missense Mutation	AAT,GAT	N648D	XP_016872429.1
XM_017016941.1	2848	Missense Mutation	AAT,GAT	N648D	XP_016872430.1
XM_017016942.1	2848	Missense Mutation	AAT,GAT	N623D	XP_016872431.1
XM_017016943.1	2848	Missense Mutation	AAT,GAT	N623D	XP_016872432.1
XM_017016944.1	2848	Missense Mutation	AAT,GAT	N623D	XP_016872433.1
XM_017016945.1	2848	Missense Mutation	AAT,GAT	N604D	XP_016872434.1
XM_017016946.1	2848	Missense Mutation	AAT,GAT	N523D	XP_016872435.1

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