Related gene-specific medical variations for Gene (Select 6894) - ClinVar

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Links from Gene

Items: 35

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3324401	NM_005646.4(TARBP1):c.46C>T (p.Pro16Ser)	LOC129932799, TARBP1 (P16S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324400	NM_005646.4(TARBP1):c.380A>G (p.Asp127Gly)	LOC129932799, TARBP1 (D127G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3173857	NM_005646.4(TARBP1):c.554A>T (p.Glu185Val)	LOC129932799, TARBP1 (E185V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3173856	NM_005646.4(TARBP1):c.52G>A (p.Ala18Thr)	LOC129932799, TARBP1 (A18T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3173836	NM_005646.4(TARBP1):c.191T>C (p.Val64Ala)	LOC129932799, TARBP1 (V64A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3173835	NM_005646.4(TARBP1):c.172C>A (p.Pro58Thr)	LOC129932799, TARBP1 (P58T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3173833	NM_005646.4(TARBP1):c.155G>C (p.Gly52Ala)	LOC129932799, TARBP1 (G52A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3173829	NM_005646.4(TARBP1):c.125G>T (p.Arg42Leu)	LOC129932799, TARBP1 (R42L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2640092	NM_005646.4(TARBP1):c.372G>A (p.Ala124=)	LOC129932799, TARBP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2615210	NM_005646.4(TARBP1):c.787T>C (p.Trp263Arg)	LOC129932799, TARBP1 (W263R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605402	NM_005646.4(TARBP1):c.277C>A (p.Arg93Ser)	LOC129932799, TARBP1 (R93S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557152	NM_005646.4(TARBP1):c.341C>T (p.Pro114Leu)	LOC129932799, TARBP1 (P114L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543692	NM_005646.4(TARBP1):c.314G>A (p.Arg105His)	LOC129932799, TARBP1 (R105H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513055	NM_005646.4(TARBP1):c.262C>A (p.Leu88Met)	LOC129932799, TARBP1 (L88M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510037	NM_005646.4(TARBP1):c.73C>G (p.Gln25Glu)	LOC129932799, TARBP1 (Q25E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459537	NM_005646.4(TARBP1):c.664G>C (p.Gly222Arg)	LOC129932799, TARBP1 (G222R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459536	NM_005646.4(TARBP1):c.563C>T (p.Ala188Val)	LOC129932799, TARBP1 (A188V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459535	NM_005646.4(TARBP1):c.271C>T (p.Arg91Cys)	LOC129932799, TARBP1 (R91C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395526	NM_005646.4(TARBP1):c.505G>A (p.Ala169Thr)	LOC129932799, TARBP1 (A169T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379143	NM_005646.4(TARBP1):c.40C>T (p.Arg14Trp)	LOC129932799, TARBP1 (R14W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363704	NM_005646.4(TARBP1):c.577G>C (p.Gly193Arg)	LOC129932799, TARBP1 (G193R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361687	NM_005646.4(TARBP1):c.484C>G (p.Arg162Gly)	LOC129932799, TARBP1 (R162G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350330	NM_005646.4(TARBP1):c.50G>A (p.Arg17Gln)	LOC129932799, TARBP1 (R17Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343315	NM_005646.4(TARBP1):c.229C>A (p.Arg77Ser)	LOC129932799, TARBP1 (R77S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342883	NM_005646.4(TARBP1):c.225C>A (p.Ser75Arg)	LOC129932799, TARBP1 (S75R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327395	NM_005646.4(TARBP1):c.83C>T (p.Ala28Val)	LOC129932799, TARBP1 (A28V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306523	NM_005646.4(TARBP1):c.520G>A (p.Gly174Arg)	LOC129932799, TARBP1 (G174R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303957	NM_005646.4(TARBP1):c.485G>T (p.Arg162Leu)	LOC129932799, TARBP1 (R162L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266841	NM_005646.4(TARBP1):c.544G>A (p.Gly182Arg)	LOC129932799, TARBP1 (G182R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266213	NM_005646.4(TARBP1):c.36G>C (p.Gln12His)	LOC129932799, TARBP1 (Q12H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254895	NM_005646.4(TARBP1):c.704C>G (p.Ala235Gly)	LOC129932799, TARBP1 (A235G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246690	NM_005646.4(TARBP1):c.731C>T (p.Pro244Leu)	LOC129932799, TARBP1 (P244L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232557	NM_005646.4(TARBP1):c.433G>C (p.Ala145Pro)	LOC129932799, TARBP1 (A145P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230224	NM_005646.4(TARBP1):c.677T>G (p.Val226Gly)	LOC129932799, TARBP1 (V226G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220587	NM_005646.4(TARBP1):c.782G>C (p.Arg261Pro)	LOC129932799, TARBP1 (R261P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Links from Gene

Items: 35