"Ambry Genetics"[submitter] AND "SERPINB11"[gene] - ClinVar

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Items: 38

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2368163	NM_001370475.1(SERPINB11):c.26T>C (p.Val9Ala)	SERPINB11 (V9A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2624144	NM_001370475.1(SERPINB11):c.55C>G (p.Leu19Val)	SERPINB11 (L19V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2530018	NM_001370475.1(SERPINB11):c.62G>A (p.Ser21Asn)	SERPINB11 (S21N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2242625	NM_001370475.1(SERPINB11):c.80A>T (p.Asn27Ile)	SERPINB11 (N27I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160393	NM_001370475.1(SERPINB11):c.88T>G (p.Phe30Val)	SERPINB11 (F30V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160384	NM_001370475.1(SERPINB11):c.121A>G (p.Met41Val)	SERPINB11 (M41V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3317588	NM_001370475.1(SERPINB11):c.139A>G (p.Arg47Gly)	SERPINB11 (R47G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160385	NM_001370475.1(SERPINB11):c.161T>G (p.Leu54Trp)	SERPINB11 (L54W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2302179	NM_001370475.1(SERPINB11):c.169G>C (p.Val57Leu)	SERPINB11 (V57L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3317586	NM_001370475.1(SERPINB11):c.229T>C (p.Cys77Arg)	SERPINB11 (C77R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2592778	NM_001370475.1(SERPINB11):c.277C>G (p.Gln93Glu)	SERPINB11 (Q93E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160386	NM_001370475.1(SERPINB11):c.346G>T (p.Ala116Ser)	SERPINB11 (A2S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2389296	NM_001370475.1(SERPINB11):c.367A>G (p.Ser123Gly)	SERPINB11 (S123G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160387	NM_001370475.1(SERPINB11):c.434C>T (p.Thr145Met)	SERPINB11 (T31M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2344700	NM_001370475.1(SERPINB11):c.434C>G (p.Thr145Arg)	SERPINB11 (T145R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160388	NM_001370475.1(SERPINB11):c.442A>C (p.Thr148Pro)	SERPINB11 (T148P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160389	NM_001370475.1(SERPINB11):c.523G>C (p.Val175Leu)	SERPINB11 (V175L +1 more)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2472109	NM_001370475.1(SERPINB11):c.545T>C (p.Ile182Thr)	SERPINB11 (I182T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2205315	NM_001370475.1(SERPINB11):c.584G>A (p.Arg195Lys)	SERPINB11 (R195K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160390	NM_001370475.1(SERPINB11):c.614G>A (p.Ser205Asn)	SERPINB11 (S205N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2461743	NM_001370475.1(SERPINB11):c.634G>A (p.Val212Met)	SERPINB11 (V212M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221637	NM_001370475.1(SERPINB11):c.686C>T (p.Pro229Leu)	SERPINB11 (P229L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160391	NM_001370475.1(SERPINB11):c.707T>C (p.Leu236Pro)	SERPINB11 (L236P +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356820	NM_001370475.1(SERPINB11):c.731G>A (p.Ser244Asn)	SERPINB11 (S157N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388823	NM_001370475.1(SERPINB11):c.751G>A (p.Val251Ile)	SERPINB11 (V76I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160392	NM_001370475.1(SERPINB11):c.794C>T (p.Ser265Leu)	SERPINB11 (S178L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317587	NM_001370475.1(SERPINB11):c.800C>T (p.Thr267Met)	SERPINB11 (T180M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516151	NM_001370475.1(SERPINB11):c.805C>A (p.His269Asn)	SERPINB11 (H182N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389803	NM_001370475.1(SERPINB11):c.833T>C (p.Met278Thr)	SERPINB11 (M103T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249722	NM_001370475.1(SERPINB11):c.839G>C (p.Arg280Thr)	SERPINB11 (R105T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533237	NM_001370475.1(SERPINB11):c.860C>A (p.Pro287His)	SERPINB11 (P112H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348930	NM_001370475.1(SERPINB11):c.922G>T (p.Asp308Tyr)	SERPINB11 (D133Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314073	NM_001370475.1(SERPINB11):c.970A>G (p.Lys324Glu)	SERPINB11 (K149E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160383	NM_001370475.1(SERPINB11):c.1028G>T (p.Gly343Val)	SERPINB11 (G343V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359559	NM_001370475.1(SERPINB11):c.1085G>T (p.Arg362Ile)	SERPINB11 (R187I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328590	NM_001370475.1(SERPINB11):c.1088C>T (p.Ala363Val)	SERPINB11 (A363V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317589	NM_001370475.1(SERPINB11):c.1099G>A (p.Ala367Thr)	SERPINB11 (A280T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538185	NM_001370475.1(SERPINB11):c.1133C>T (p.Thr378Ile)	SERPINB11 (T203I +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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Items: 38