List of variants in gene combination LOC129934333, TMEM127 reported as uncertain significance for endocrine gland neoplasm

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 24

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HGVS	dbSNP	gnomAD frequency
NM_017849.4(TMEM127):c.88A>G (p.Ser30Gly)	rs763476625	0.00010
NM_017849.4(TMEM127):c.49A>G (p.Ser17Gly)	rs1249001227	0.00008
NM_017849.4(TMEM127):c.121A>G (p.Ile41Val)	rs760633411	0.00006
NM_017849.4(TMEM127):c.52C>T (p.Pro18Ser)	rs1452142786	0.00002
NM_017849.4(TMEM127):c.80C>T (p.Pro27Leu)	rs983504110	0.00002
NM_017849.4(TMEM127):c.101C>G (p.Ala34Gly)	rs1451389209	0.00001
NM_017849.4(TMEM127):c.10C>T (p.Pro4Ser)	rs1024081498	0.00001
NM_017849.4(TMEM127):c.12C>T (p.Pro4=)	rs1406470818	0.00001
NM_017849.4(TMEM127):c.62G>A (p.Ser21Asn)	rs1348645128	0.00001
NM_017849.4(TMEM127):c.67C>A (p.Leu23Met)	rs749807415	0.00001
NM_017849.4(TMEM127):c.-114C>T	rs1684402630
NM_017849.4(TMEM127):c.-131-7C>T	rs886056450
NM_017849.4(TMEM127):c.-37A>G	rs886056449
NM_017849.4(TMEM127):c.110G>A (p.Gly37Asp)
NM_017849.4(TMEM127):c.112G>T (p.Ala38Ser)	rs1456398772
NM_017849.4(TMEM127):c.13G>A (p.Gly5Arg)	rs786202314
NM_017849.4(TMEM127):c.17G>T (p.Gly6Val)
NM_017849.4(TMEM127):c.24_32del (p.Leu9_Gly11del)	rs1684396239
NM_017849.4(TMEM127):c.29C>T (p.Pro10Leu)
NM_017849.4(TMEM127):c.37C>T (p.Arg13Cys)
NM_017849.4(TMEM127):c.44G>T (p.Arg15Leu)	rs2104308338
NM_017849.4(TMEM127):c.50G>T (p.Ser17Ile)	rs1223613323
NM_017849.4(TMEM127):c.59G>T (p.Gly20Val)
NM_017849.4(TMEM127):c.61A>T (p.Ser21Cys)

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