Product Details

SNP ID

rs199663756

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:99612548 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATAGGTTGAGGAATCATTACCTTCC[A/G]CAGGGTTCATGGCTGCATCATGAAG

Phenotype

MIM: 609767

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC25A28 PubMed Links

Gene Details

Gene

SLC25A28

Gene Name

solute carrier family 25 member 28

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_031212.3	587	Missense Mutation	GCG,GTG	A191V	NP_112489.3
XM_005270208.1	587	Missense Mutation	GCG,GTG	A92V	XP_005270265.1
XM_005270211.4	587	Missense Mutation	GCG,GTG	A92V	XP_005270268.1
XM_006718005.3	587	Missense Mutation	GCG,GTG	A92V	XP_006718068.1
XM_006718006.3	587	Missense Mutation	GCG,GTG	A191V	XP_006718069.1
XM_011540239.2	587	Missense Mutation	GCG,GTG	A101V	XP_011538541.1
XM_011540240.1	587	Missense Mutation	GCG,GTG	A92V	XP_011538542.1
XM_011540244.2	587	Missense Mutation	GCG,GTG	A191V	XP_011538546.1
XM_017016741.1	587	Missense Mutation	GCG,GTG	A92V	XP_016872230.1
XM_017016742.1	587	Missense Mutation	GCG,GTG	A36V	XP_016872231.1

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