List of variants in gene KANSL1 reported as benign by Athena Diagnostics Inc

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: 18

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HGVS	dbSNP
NM_001193466.2(KANSL1):c.1491A>G (p.Pro497=)	rs17576165
NM_001193466.2(KANSL1):c.1652C>T (p.Thr551Ile)	rs778178483
NM_001193466.2(KANSL1):c.1653-10C>G	rs199642265
NM_001193466.2(KANSL1):c.1826G>A (p.Ser609Asn)	rs138698439
NM_001193466.2(KANSL1):c.1938C>T (p.Pro646=)	rs371047711
NM_001193466.2(KANSL1):c.2109A>G (p.Leu703=)	rs34101027
NM_001193466.2(KANSL1):c.2152T>C (p.Ser718Pro)	rs34043286
NM_001193466.2(KANSL1):c.2580T>C (p.Phe860=)	rs17574604
NM_001193466.2(KANSL1):c.311A>C (p.Lys104Thr)	rs17585974
NM_001193466.2(KANSL1):c.3170A>G (p.Gln1057Arg)	rs201083879
NM_001193466.2(KANSL1):c.414T>G (p.Leu138=)	rs17662889
NM_001193466.2(KANSL1):c.607G>C (p.Gly203Arg)	rs138175526
NM_001193466.2(KANSL1):c.673A>G (p.Asn225Asp)	rs35643216
NM_001193466.2(KANSL1):c.680G>A (p.Ser227Asn)	rs150345690
NM_001193466.2(KANSL1):c.696C>T (p.Ser232=)	rs1881194
NM_001193466.2(KANSL1):c.727C>A (p.Gln243Lys)	rs142096969
NM_001193466.2(KANSL1):c.741A>G (p.Arg247=)	rs1881193
NM_001193466.2(KANSL1):c.773T>C (p.Leu258Ser)	rs145714368

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