List of variants in gene FAM149B1 reported as uncertain significance for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_173348.2(FAM149B1):c.2T>G (p.Met1Arg)	rs569932117	0.00080
NM_173348.2(FAM149B1):c.1022C>T (p.Pro341Leu)	rs536760754	0.00032
NM_173348.2(FAM149B1):c.1068T>G (p.Asp356Glu)	rs554018296	0.00023
NM_173348.2(FAM149B1):c.515C>A (p.Thr172Asn)	rs370830764	0.00007
NM_173348.2(FAM149B1):c.789T>G (p.Phe263Leu)	rs375715642	0.00003
NM_173348.2(FAM149B1):c.518T>C (p.Leu173Ser)	rs1487614258	0.00002
NM_173348.2(FAM149B1):c.848T>C (p.Val283Ala)	rs558516290	0.00002
NM_173348.2(FAM149B1):c.1079A>G (p.His360Arg)	rs767041717	0.00001
NM_173348.2(FAM149B1):c.166A>G (p.Thr56Ala)	rs781131842	0.00001
NM_173348.2(FAM149B1):c.173A>C (p.Glu58Ala)	rs1021125981	0.00001
NM_173348.2(FAM149B1):c.187T>G (p.Ser63Ala)	rs1171894836	0.00001
NM_173348.2(FAM149B1):c.55A>T (p.Ile19Leu)	rs1357373262	0.00001
NM_173348.2(FAM149B1):c.713A>T (p.Glu238Val)	rs1398498062	0.00001
NM_173348.2(FAM149B1):c.1004T>C (p.Leu335Pro)
NM_173348.2(FAM149B1):c.1023G>C (p.Pro341=)	rs780876261
NM_173348.2(FAM149B1):c.1093C>G (p.Gln365Glu)	rs753919394
NM_173348.2(FAM149B1):c.1106T>G (p.Leu369Arg)	rs2493298366
NM_173348.2(FAM149B1):c.1117G>C (p.Asp373His)
NM_173348.2(FAM149B1):c.179C>G (p.Ser60Cys)	rs1749244375
NM_173348.2(FAM149B1):c.349G>A (p.Glu117Lys)
NM_173348.2(FAM149B1):c.410G>A (p.Ser137Asn)	rs2042713434
NM_173348.2(FAM149B1):c.413T>G (p.Phe138Cys)	rs1239830024
NM_173348.2(FAM149B1):c.448A>C (p.Thr150Pro)
NM_173348.2(FAM149B1):c.499G>A (p.Ala167Thr)	rs61740304
NM_173348.2(FAM149B1):c.515C>T (p.Thr172Ile)	rs370830764
NM_173348.2(FAM149B1):c.602C>G (p.Ser201Cys)
NM_173348.2(FAM149B1):c.906G>C (p.Glu302Asp)
NM_173348.2(FAM149B1):c.917C>A (p.Ala306Glu)	rs1326816660

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