Product Details

SNP ID: rs3746107
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.19:1250398 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCGAGGCGGCGCCCATGAGCCTCGC[C/T]ATCCACAGCACCACGGGCACCCGCT
Phenotype: MIM: 603150 MIM: 606700
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: ATP5D PubMed Links

Gene Details

Gene: ATP5D
Gene Name: ATP synthase, H+ transporting, mitochondrial F1 complex, delta subunit

There are no transcripts associated with this gene.

Gene: MIDN
Gene Name: midnolin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_177401.4	617	Silent Mutation	GCC,GCT	A34A	NP_796375.3
XM_005259671.3	617	Silent Mutation	GCC,GCT	A34A	XP_005259728.1
XM_005259672.3	617	Silent Mutation	GCC,GCT	A34A	XP_005259729.1

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