List of variants in gene TMPO 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: 27

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HGVS	dbSNP	gnomAD frequency
NM_001032283.3(TMPO):c.565+1696C>T	rs141443652	0.00142
NM_001032283.3(TMPO):c.565+2149C>T	rs34150443	0.00064
NM_001032283.3(TMPO):c.565+2368G>A	rs138295270	0.00058
NM_001032283.3(TMPO):c.565+1848G>A	rs34301677	0.00037
NM_001032283.3(TMPO):c.806G>A (p.Arg269His)	rs142891873	0.00017
NM_001032283.3(TMPO):c.565+1641A>G	rs143232629	0.00011
NM_001032283.3(TMPO):c.565+1328G>T	rs369208265	0.00006
NM_001032283.3(TMPO):c.614G>A (p.Arg205Lys)	rs727504952	0.00004
NM_001032283.3(TMPO):c.1174C>T (p.Pro392Ser)	rs727504622	0.00003
NM_001032283.3(TMPO):c.565+1917A>G	rs727505217	0.00003
NM_001032283.3(TMPO):c.70A>C (p.Asn24His)	rs727505279	0.00002
NM_001032283.3(TMPO):c.565+1137G>A	rs375903462	0.00001
NM_001032283.3(TMPO):c.565+1275A>G	rs763320036	0.00001
NM_001032283.3(TMPO):c.565+1606C>T	rs727505047	0.00001
NM_001032283.3(TMPO):c.565+2178G>A	rs1343917914	0.00001
NM_001032283.3(TMPO):c.190G>A (p.Asp64Asn)	rs1462361337
NM_001032283.3(TMPO):c.19G>C (p.Asp7His)
NM_001032283.3(TMPO):c.565+1242A>G
NM_001032283.3(TMPO):c.565+1548A>G	rs779658294
NM_001032283.3(TMPO):c.565+1777G>C
NM_001032283.3(TMPO):c.565+1819A>G	rs1479099731
NM_001032283.3(TMPO):c.565+1983del
NM_001032283.3(TMPO):c.565+2138T>G
NM_001032283.3(TMPO):c.565+2296C>T	rs397516843
NM_001032283.3(TMPO):c.565+2461_565+2463del	rs727503491
NM_001032283.3(TMPO):c.77C>T (p.Thr26Met)	rs397516494
NM_001032283.3(TMPO):c.991-14_991-11del	rs397516495

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