Related gene-specific medical variations for Gene (Select 219743) - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3330439	NM_173555.4(TYSND1):c.398A>G (p.Glu133Gly)	LOC130003996, TYSND1 (E133G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330438	NM_173555.4(TYSND1):c.947G>A (p.Ser316Asn)	LOC130003994, TYSND1 (S316N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330436	NM_173555.4(TYSND1):c.933C>A (p.His311Gln)	LOC130003994, TYSND1 (H311Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185285	NM_173555.4(TYSND1):c.852T>G (p.Cys284Trp)	LOC130003994, TYSND1 (C284W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185283	NM_173555.4(TYSND1):c.356C>G (p.Ala119Gly)	LOC130003996, TYSND1 (A119G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185282	NM_173555.4(TYSND1):c.320C>A (p.Thr107Lys)	LOC130003996, TYSND1 (T107K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185281	NM_173555.4(TYSND1):c.317G>A (p.Cys106Tyr)	LOC130003996, TYSND1 (C106Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185280	NM_173555.4(TYSND1):c.263C>T (p.Ala88Val)	LOC130003996, TYSND1 (A88V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559874	NM_173555.4(TYSND1):c.311G>A (p.Gly104Glu)	LOC130003996, TYSND1 (G104E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540217	NM_173555.4(TYSND1):c.924C>A (p.Asp308Glu)	LOC130003994, TYSND1 (D308E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479506	NM_173555.4(TYSND1):c.803C>T (p.Thr268Ile)	LOC130003994, TYSND1 (T268I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403259	NM_173555.4(TYSND1):c.764C>T (p.Ala255Val)	LOC130003994, TYSND1 (A255V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320557	NM_173555.4(TYSND1):c.974C>T (p.Pro325Leu)	LOC130003994, TYSND1 (P325L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294139	NM_173555.4(TYSND1):c.397G>A (p.Glu133Lys)	LOC130003996, TYSND1 (E133K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291362	NM_173555.4(TYSND1):c.338T>G (p.Leu113Arg)	LOC130003996, TYSND1 (L113R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290853	NM_173555.4(TYSND1):c.322C>T (p.Pro108Ser)	LOC130003996, TYSND1 (P108S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228427	NM_173555.4(TYSND1):c.958C>G (p.Leu320Val)	LOC130003994, TYSND1 (L320V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 774893	NM_173555.4(TYSND1):c.338T>C (p.Leu113Pro)	LOC130003996, TYSND1 (L113P)	Single nucleotide variant (missense variant)	not provided	GBenign