Product Details

SNP ID

rs140723918

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:1254928 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGATGGACTGCTCCCCCACGGCCAG[C/T]AGCAGTGCCAGTCCTGGTGCCAGCA

Phenotype

MIM: 606700

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MIDN PubMed Links

Gene Details

Gene

MIDN

Gene Name

midnolin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_177401.4	1367	Silent Mutation	AGC,AGT	S241S	NP_796375.3
XM_005259671.3	1367	Missense Mutation	AGC,AGT	S284S	XP_005259728.1
XM_005259672.3	1367	Missense Mutation	AGC,AGT	S283S	XP_005259729.1

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