Variant Term Annotation Report - Rat Genome Database

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VARIANT - TERM ANNOTATION REPORT

RGD ID:	8617338
Species:	Homo sapiens
RGD Object:	Variant
Symbol:	CV71249
Name:	NM_017739.4(POMGNT1):c.931C>T (p.Arg311Ter)

Acc ID:	DOID:9008630
Term:	Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 3
Definition:	null

Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.

Object Symbol

Qualifier

Evidence

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Reference

Source

Notes

Original Reference(s)

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.