List of variants in gene RPS6KC1 reported as benign for not provided

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_012424.6(RPS6KC1):c.2559G>T (p.Leu853Phe)	rs34080597	0.03281
NM_012424.6(RPS6KC1):c.1636G>C (p.Ala546Pro)	rs35281247	0.01138
NM_012424.6(RPS6KC1):c.956C>T (p.Pro319Leu)	rs56369827	0.01063
NM_012424.6(RPS6KC1):c.1724A>G (p.Asn575Ser)	rs56060894	0.00647
NM_012424.6(RPS6KC1):c.105+9C>T	rs113940805	0.00561
NM_012424.6(RPS6KC1):c.3033C>T (p.His1011=)	rs34661072	0.00458
NM_012424.6(RPS6KC1):c.835+18T>C	rs139986699	0.00388
NM_012424.6(RPS6KC1):c.1682C>G (p.Pro561Arg)	rs17020314	0.00306
NM_012424.6(RPS6KC1):c.622G>T (p.Ala208Ser)	rs139296657	0.00245
NM_012424.6(RPS6KC1):c.836-11T>C	rs200774550	0.00192
NM_012424.6(RPS6KC1):c.610C>G (p.Leu204Val)	rs141240814	0.00156
NM_012424.6(RPS6KC1):c.2886C>T (p.Ala962=)	rs147823242	0.00145
NM_012424.6(RPS6KC1):c.3091-13C>T	rs181418262	0.00143
NM_012424.6(RPS6KC1):c.1560G>A (p.Gly520=)	rs139110232	0.00066
NM_012424.6(RPS6KC1):c.1225+8T>G	rs187492406	0.00056
NM_012424.6(RPS6KC1):c.2745A>G (p.Val915=)	rs562923473	0.00040
NM_012424.6(RPS6KC1):c.2472A>C (p.Pro824=)	rs199581175	0.00020
NM_012424.6(RPS6KC1):c.1045-11C>T	rs201214518	0.00006
NM_012424.6(RPS6KC1):c.1002C>T (p.Ala334=)
NM_012424.6(RPS6KC1):c.106-18A>C	rs79466500
NM_012424.6(RPS6KC1):c.106-18A>G	rs79466500
NM_012424.6(RPS6KC1):c.285C>A (p.Ile95=)	rs56056039
NM_012424.6(RPS6KC1):c.3091-3dup
NM_012424.6(RPS6KC1):c.472+4_472+6dup	rs541997155
NM_012424.6(RPS6KC1):c.836-3del	rs567683596
NM_012424.6(RPS6KC1):c.836-3dup

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