TFB1M[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2464342	NM_016020.4(TFB1M):c.935A>G (p.Asp312Gly)	TFB1M (D217G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3176471	NM_016020.4(TFB1M):c.916G>A (p.Val306Ile)	TFB1M (V211I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3176470	NM_016020.4(TFB1M):c.878G>A (p.Arg293His)	TFB1M (R198H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3176469	NM_016020.4(TFB1M):c.817C>T (p.Arg273Cys)	TFB1M (R273C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2402738	NM_016020.4(TFB1M):c.785G>A (p.Arg262Gln)	TFB1M (R262Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304507	NM_016020.4(TFB1M):c.655C>T (p.Pro219Ser)	TFB1M (P124S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2341714	NM_016020.4(TFB1M):c.620G>A (p.Arg207Gln)	TFB1M (R207Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2297570	NM_016020.4(TFB1M):c.595A>G (p.Met199Val)	TFB1M (M199V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2405946	NM_016020.4(TFB1M):c.578G>A (p.Arg193His)	TFB1M (R98H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2478802	NM_016020.4(TFB1M):c.424C>A (p.Leu142Met)	TFB1M (L142M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2375376	NM_016020.4(TFB1M):c.404A>G (p.Asn135Ser)	TFB1M (N40S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3176468	NM_016020.4(TFB1M):c.322G>A (p.Val108Ile)	TFB1M (V13I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2489931	NM_016020.4(TFB1M):c.290T>G (p.Leu97Arg)	TFB1M (L2R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2532576	NM_016020.4(TFB1M):c.213A>T (p.Arg71Ser)	TFB1M (R71S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 710998	NM_016020.4(TFB1M):c.180C>T (p.Tyr60=)	TFB1M	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 2533586	NM_016020.4(TFB1M):c.170C>T (p.Ala57Val)	TFB1M (A57V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance