Related gene-specific medical variations for Gene (Select 11103) - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3289320	NM_007043.7(KRR1):c.839A>G (p.Lys280Arg)	GLIPR1, KRR1 (K280R)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3281578	NM_006851.3(GLIPR1):c.626G>A (p.Arg209Gln)	KRR1, GLIPR1 (R209Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3116295	NM_007043.7(KRR1):c.887G>A (p.Arg296Gln)	GLIPR1, KRR1 (R296Q)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2623451	NM_006851.3(GLIPR1):c.557A>G (p.Tyr186Cys)	GLIPR1, KRR1 (Y186C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2555829	NM_006851.3(GLIPR1):c.748A>G (p.Ile250Val)	GLIPR1, KRR1 (I250V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528736	NM_007043.7(KRR1):c.1073T>C (p.Leu358Pro)	GLIPR1, KRR1 (L358P)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2475725	NM_007043.7(KRR1):c.911C>A (p.Ala304Asp)	GLIPR1, KRR1 (A304D)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2475399	NM_007043.7(KRR1):c.932G>T (p.Ser311Ile)	GLIPR1, KRR1 (S311I)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2384080	NM_006851.3(GLIPR1):c.600G>C (p.Lys200Asn)	GLIPR1, KRR1 (K200N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2381594	NM_006851.3(GLIPR1):c.547A>G (p.Thr183Ala)	GLIPR1, KRR1 (T183A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2371786	NM_007043.7(KRR1):c.902C>T (p.Ala301Val)	GLIPR1, KRR1 (A301V)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2371622	NM_007043.7(KRR1):c.904A>G (p.Ile302Val)	GLIPR1, KRR1 (I302V)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2333384	NM_006851.3(GLIPR1):c.689G>C (p.Arg230Pro)	GLIPR1, KRR1 (R230P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2312049	NM_006851.3(GLIPR1):c.716T>C (p.Ile239Thr)	GLIPR1, KRR1 (I239T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2297797	NM_007043.7(KRR1):c.847G>A (p.Ala283Thr)	GLIPR1, KRR1 (A283T)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 784249	NM_006851.3(GLIPR1):c.534-5T>C	GLIPR1, KRR1	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign