List of variants in gene CLTC reported as likely benign for CLTC-related disorder

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_004859.4(CLTC):c.87C>T (p.Thr29=)	rs139085965	0.00108
NM_004859.4(CLTC):c.1522-8G>C	rs377049407	0.00085
NM_004859.4(CLTC):c.18A>C (p.Pro6=)	rs76471984	0.00034
NM_004859.4(CLTC):c.1029A>G (p.Gln343=)	rs146333268	0.00033
NM_004859.4(CLTC):c.3333T>A (p.Leu1111=)	rs145280858	0.00023
NM_004859.4(CLTC):c.2562-5C>T	rs200170084	0.00017
NM_004859.4(CLTC):c.4722C>T (p.Tyr1574=)	rs367867382	0.00009
NM_004859.4(CLTC):c.4904-8T>G	rs367691240	0.00009
NM_004859.4(CLTC):c.4980C>T (p.Thr1660=)	rs199812583	0.00007
NM_004859.4(CLTC):c.3762A>G (p.Lys1254=)	rs111452880	0.00005
NM_004859.4(CLTC):c.3096A>C (p.Ala1032=)	rs150533662	0.00004
NM_004859.4(CLTC):c.*6A>G	rs941861509	0.00001
NM_004859.4(CLTC):c.1947+8A>T	rs1273358811	0.00001
NM_004859.4(CLTC):c.*9G>A
NM_004859.4(CLTC):c.1920G>C (p.Val640=)	rs2032738501
NM_004859.4(CLTC):c.2562-19TTTTTTCC[3]	rs2032979421
NM_004859.4(CLTC):c.4903+5TC[2]	rs758438882

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