List of variants in gene TMEM127 reported as benign for benign neoplasm

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_017849.4(TMEM127):c.*1958A>C	rs7058	0.56373
NM_017849.4(TMEM127):c.621G>A (p.Ala207=)	rs3852673	0.13717
NM_017849.4(TMEM127):c.*338G>A	rs13022177	0.03241
NM_017849.4(TMEM127):c.*1301T>C	rs3770239	0.01488
NM_017849.4(TMEM127):c.*2086C>T	rs13418193	0.00895
NM_017849.4(TMEM127):c.*1163C>T	rs11691019	0.00769
NM_017849.4(TMEM127):c.*50C>T	rs72937654	0.00712
NM_017849.4(TMEM127):c.*2012C>T	rs149122699	0.00641
NM_017849.4(TMEM127):c.409+7C>T	rs189327749	0.00487
NM_017849.4(TMEM127):c.*1306C>T	rs148119945	0.00371
NM_017849.4(TMEM127):c.*2498C>T	rs191565203	0.00173
NM_017849.4(TMEM127):c.*2845T>G	rs182729595	0.00168
NM_017849.4(TMEM127):c.*1233C>T	rs536712285	0.00162
NM_017849.4(TMEM127):c.*2300G>A	rs117655540	0.00153
NM_017849.4(TMEM127):c.*502C>T	rs191970829	0.00128
NM_017849.4(TMEM127):c.*57C>T	rs147532087	0.00089
NM_017849.4(TMEM127):c.*3209A>G	rs186348610	0.00064
NM_017849.4(TMEM127):c.*2966C>G	rs17119378	0.00049
NM_017849.4(TMEM127):c.565C>T (p.Leu189=)	rs146965678	0.00022
NM_017849.4(TMEM127):c.*3569C>T	rs140274612	0.00020
NM_017849.4(TMEM127):c.*3584G>C	rs370166706	0.00009
NM_017849.4(TMEM127):c.*1723C>T	rs551200730	0.00005
NM_017849.4(TMEM127):c.*1505A>G	rs118172849	0.00002
NM_017849.4(TMEM127):c.394G>A (p.Ala132Thr)	rs750870974	0.00001
NM_017849.4(TMEM127):c.534C>T (p.Tyr178=)	rs550833832	0.00001
NM_017849.4(TMEM127):c.*1772G>A	rs537225254

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