Product Details

SNP ID

rs150416544

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:112540915 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGATTGAATCAGCTTGAGTGTAAAC[A/G]TAGCTTCTGCCACATTATGAAAGCT

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ZGRF1 PubMed Links

Gene Details

Gene

ZGRF1

Gene Name

zinc finger GRF-type containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018392.4	5976	Missense Mutation	ACG,ATG	T1939M	NP_060862.3
XM_005263115.3	5976	Missense Mutation	ACG,ATG	T1939M	XP_005263172.1
XM_011532091.2	5976	Missense Mutation	ACG,ATG	T1922M	XP_011530393.1
XM_011532092.2	5976	Missense Mutation	ACG,ATG	T1919M	XP_011530394.1
XM_011532093.2	5976	Missense Mutation	ACG,ATG	T1881M	XP_011530395.1
XM_011532094.2	5976	Missense Mutation	ACG,ATG	T1853M	XP_011530396.1
XM_011532096.2	5976	Intron			XP_011530398.1
XM_011532097.2	5976	Missense Mutation	ACG,ATG	T988M	XP_011530399.1
XM_011532098.2	5976	Missense Mutation	ACG,ATG	T896M	XP_011530400.1
XM_011532099.2	5976	Missense Mutation	ACG,ATG	T896M	XP_011530401.1
XM_017008369.1	5976	Missense Mutation	ACG,ATG	T1919M	XP_016863858.1
XM_017008370.1	5976	Missense Mutation	ACG,ATG	T1864M	XP_016863859.1
XM_017008371.1	5976	Missense Mutation	ACG,ATG	T1844M	XP_016863860.1
XM_017008372.1	5976	Missense Mutation	ACG,ATG	T689M	XP_016863861.1
XM_017008373.1	5976	Missense Mutation	ACG,ATG	T689M	XP_016863862.1

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