Related gene-specific medical variations for Gene (Select 2918) - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685268	GRCh37/hg19 7q31.33(chr7:126642908-126848563)x1	GRM8	Copy number loss	not provided	GUncertain significance
Select item 2685267	GRCh37/hg19 7q31.33(chr7:126384827-126506598)x1	GRM8	Copy number loss	not provided	GUncertain significance
Select item 2685265	GRCh37/hg19 7q31.33(chr7:126362379-126421341)x1	GRM8	Copy number loss	not provided	GUncertain significance
Select item 1808279	GRCh37/hg19 7q31.33(chr7:125593340-126417532)x3	GRM8	Copy number gain	not provided	GUncertain significance
Select item 1707621	GRCh37/hg19 7q31.33(chr7:126392370-126446732)x1	GRM8	Copy number loss	Syndromic anorectal malformation	GUncertain significance
Select item 1341267	GRCh37/hg19 7q31.33(chr7:125387232-126441223)x1	GRM8	Copy number loss	not provided	GLikely benign
Select item 689095	GRCh37/hg19 7q31.33(chr7:125898014-126173095)x1	GRM8	Copy number loss	not provided	GUncertain significance
Select item 687151	GRCh37/hg19 7q31.33(chr7:125898014-126173095)x1	GRM8	Copy number loss	not provided	GUncertain significance
Select item 686076	GRCh37/hg19 7q31.33(chr7:125893482-126140769)x3	GRM8	Copy number gain	not provided	GUncertain significance
Select item 685289	GRCh37/hg19 7q31.33(chr7:126046601-126086288)x1	GRM8	Copy number loss	not provided	GUncertain significance
Select item 563288	GRCh37/hg19 7q31.33(chr7:126384826-126463292)x1	GRM8	Copy number loss	not provided	GLikely benign
Select item 161472	NM_000845.3(GRM8):c.2554C>T (p.Arg852Cys)	GRM8 (R852C +1 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance