List of variants in gene MSH6 reported as benign by Quest Diagnostics Nichols Institute San Juan Capistrano

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: 37

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.431G>T (p.Ser144Ile)	rs3211299	0.00158
NM_000179.3(MSH6):c.3647-6T>A	rs182871847	0.00134
NM_000179.3(MSH6):c.984C>T (p.Ser328=)	rs138143769	0.00101
NM_000179.3(MSH6):c.3265T>C (p.Leu1089=)	rs34490141	0.00096
NM_000179.3(MSH6):c.1526T>C (p.Val509Ala)	rs63751005	0.00067
NM_000179.3(MSH6):c.1665A>G (p.Ala555=)	rs146785465	0.00066
NM_000179.3(MSH6):c.1869C>T (p.Pro623=)	rs141242295	0.00058
NM_000179.3(MSH6):c.3960A>G (p.Ala1320=)	rs373425206	0.00042
NM_000179.3(MSH6):c.1449G>T (p.Val483=)	rs35590297	0.00037
NM_000179.3(MSH6):c.3488A>T (p.Glu1163Val)	rs63750252	0.00032
NM_000179.3(MSH6):c.3217C>T (p.Pro1073Ser)	rs142254875	0.00028
NM_000179.3(MSH6):c.3438+11_3438+14del	rs377746844	0.00023
NM_000179.3(MSH6):c.2925C>T (p.Asn975=)	rs139026662	0.00016
NM_000179.3(MSH6):c.102C>A (p.Ala34=)	rs201132087	0.00013
NM_000179.3(MSH6):c.1875C>T (p.Ser625=)	rs63749886	0.00010
NM_000179.3(MSH6):c.3245C>T (p.Pro1082Leu)	rs191109849	0.00010
NM_000179.3(MSH6):c.3264C>T (p.Phe1088=)	rs35621414	0.00008
NM_000179.3(MSH6):c.2724A>G (p.Glu908=)	rs35389622	0.00006
NM_000179.3(MSH6):c.3557-3A>T	rs41295274	0.00004
NM_000179.3(MSH6):c.*17G>A	rs876661000	0.00003
NM_000179.3(MSH6):c.393A>C (p.Val131=)	rs752488540	0.00003
NM_000179.3(MSH6):c.1509C>T (p.Ser503=)	rs545020313	0.00002
NM_000179.3(MSH6):c.1776A>T (p.Val592=)	rs56132616	0.00001
NM_000179.3(MSH6):c.3300G>A (p.Thr1100=)	rs540252208	0.00001
NM_000179.3(MSH6):c.3980A>G (p.Asn1327Ser)	rs780187989	0.00001
NM_000179.3(MSH6):c.3162C>T (p.Ile1054=)	rs149605979
NM_000179.3(MSH6):c.3246G>A (p.Pro1082=)	rs3136351
NM_000179.3(MSH6):c.3246G>T (p.Pro1082=)	rs3136351
NM_000179.3(MSH6):c.3354G>A (p.Glu1118=)	rs35642130
NM_000179.3(MSH6):c.3384T>C (p.Tyr1128=)	rs544518097
NM_000179.3(MSH6):c.4002-10del	rs59056100
NM_000179.3(MSH6):c.4002-10dup	rs59056100
NM_000179.3(MSH6):c.4002-11_4002-10dup	rs59056100
NM_000179.3(MSH6):c.4002-12_4002-10dup	rs59056100
NM_000179.3(MSH6):c.4002-13_4002-10dup	rs59056100
NM_000179.3(MSH6):c.4002-8A>T	rs778957100
NM_000179.3(MSH6):c.4068_4071dup (p.Lys1358delinsAspTer)	rs55740729

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