List of variants in gene MED25 reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 31

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HGVS	dbSNP	gnomAD frequency
NM_030973.4(MED25):c.1727C>G (p.Ala576Gly)	rs193291405	0.00836
NM_030973.4(MED25):c.1004C>T (p.Ala335Val)	rs145770066	0.00443
NM_030973.4(MED25):c.93C>T (p.Tyr31=)	rs61742955	0.00394
NM_030973.4(MED25):c.2088G>A (p.Leu696=)	rs371157406	0.00252
NM_030973.4(MED25):c.396C>T (p.Arg132=)	rs142353864	0.00125
NM_030973.4(MED25):c.354C>T (p.Leu118=)	rs145574885	0.00110
NM_030973.4(MED25):c.135-6T>G	rs199743509	0.00036
NM_030973.4(MED25):c.1095G>A (p.Pro365=)	rs373128874	0.00017
NM_030973.4(MED25):c.1966C>A (p.Pro656Thr)	rs199761611	0.00014
NM_030973.4(MED25):c.942C>T (p.Pro314=)	rs373971747	0.00009
NM_030973.4(MED25):c.1101+4G>A	rs746210338	0.00007
NM_030973.4(MED25):c.1038G>T (p.Leu346=)	rs759964732	0.00006
NM_030973.4(MED25):c.1572C>T (p.Gly524=)	rs559482732	0.00005
NM_030973.4(MED25):c.1335C>T (p.Pro445=)	rs372191174	0.00004
NM_030973.4(MED25):c.678C>T (p.Leu226=)	rs770604129	0.00003
NM_030973.4(MED25):c.769C>G (p.Leu257Val)	rs1057519203	0.00002
NM_030973.4(MED25):c.135-3C>T	rs750459702	0.00001
NM_030973.4(MED25):c.1678G>C (p.Gly560Arg)	rs866498468	0.00001
NM_030973.4(MED25):c.2042C>T (p.Pro681Leu)	rs974538844	0.00001
NM_030973.4(MED25):c.384C>T (p.Phe128=)	rs1204577575	0.00001
NM_030973.4(MED25):c.526C>T (p.Arg176Trp)	rs757456871	0.00001
NM_030973.4(MED25):c.954C>T (p.Pro318=)	rs554447029	0.00001
NM_030973.4(MED25):c.1275G>A (p.Arg425=)
NM_030973.4(MED25):c.1788A>G (p.Val596=)
NM_030973.4(MED25):c.1887C>T (p.Pro629=)
NM_030973.4(MED25):c.228C>T (p.Cys76=)	rs770196362
NM_030973.4(MED25):c.377A>T (p.Asp126Val)	rs751058652
NM_030973.4(MED25):c.518T>C (p.Ile173Thr)	rs781753774
NM_030973.4(MED25):c.633A>G (p.Thr211=)	rs369117035
NM_030973.4(MED25):c.735C>T (p.Val245=)
NM_030973.4(MED25):c.908-6C>A

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