| 15190832 | CV731158 | single nucleotide variant | NM_032595.5(PPP1R9B):c.1625+7A>G | not provided [RCV000888209] | benign | 17 | 50143591 | 50143591 | Human | | name |
| 8644994 | CV104401 | single nucleotide variant | NM_032595.5(PPP1R9B):c.198G>C (p.Thr66=) | not provided [RCV000084799] | not provided | 17 | 50150316 | 50150316 | Human | | name |
| 405268400 | CV3189660 | single nucleotide variant | NM_032595.5(PPP1R9B):c.234G>C (p.Ala78=) | PPP1R9B-related disorder [RCV003899052] | likely benign | 17 | 50150280 | 50150280 | Human | | name , trait , alternate_id |
| 405264552 | CV3189976 | single nucleotide variant | NM_032595.5(PPP1R9B):c.159C>T (p.Asn53=) | PPP1R9B-related disorder [RCV003897020] | likely benign | 17 | 50150355 | 50150355 | Human | | name , trait , alternate_id |
| 405262033 | CV3194274 | single nucleotide variant | NM_032595.5(PPP1R9B):c.240G>C (p.Leu80=) | PPP1R9B-related disorder [RCV003896310] | likely benign | 17 | 50150274 | 50150274 | Human | | name , trait , alternate_id |
| 405269438 | CV3201608 | single nucleotide variant | NM_032595.5(PPP1R9B):c.222G>T (p.Ala74=) | PPP1R9B-related disorder [RCV003899518] | likely benign | 17 | 50150292 | 50150292 | Human | | name , trait , alternate_id |
| 405289706 | CV3218303 | single nucleotide variant | NM_032595.5(PPP1R9B):c.222G>C (p.Ala74=) | PPP1R9B-related disorder [RCV003983705] | likely benign | 17 | 50150292 | 50150292 | Human | | name , trait , alternate_id |
| 8644984 | CV104391 | single nucleotide variant | NM_032595.5(PPP1R9B):c.777C>G (p.Pro259=) | not provided [RCV000084789] | not provided | 17 | 50149737 | 50149737 | Human | | name |
| 8644985 | CV104392 | single nucleotide variant | NM_032595.5(PPP1R9B):c.729G>A (p.Leu243=) | not provided [RCV000084790] | not provided | 17 | 50149785 | 50149785 | Human | | name |
| 8644987 | CV104394 | single nucleotide variant | NM_032595.5(PPP1R9B):c.579C>G (p.Thr193=) | not provided [RCV000084792] | not provided | 17 | 50149935 | 50149935 | Human | | name |
| 8644988 | CV104395 | single nucleotide variant | NM_032595.5(PPP1R9B):c.513G>A (p.Leu171=) | not provided [RCV000084793] | not provided | 17 | 50150001 | 50150001 | Human | | name |
| 8644990 | CV104397 | single nucleotide variant | NM_032595.5(PPP1R9B):c.462C>T (p.Ser154=) | PPP1R9B-related disorder [RCV003964955]|not provided [RCV000084795] | likely benign|not provided | 17 | 50150052 | 50150052 | Human | | name , trait , alternate_id |
| 8644992 | CV104399 | single nucleotide variant | NM_032595.5(PPP1R9B):c.336G>A (p.Lys112=) | not provided [RCV000084797] | not provided | 17 | 50150178 | 50150178 | Human | | name |
| 155974646 | CV2342577 | single nucleotide variant | NM_032595.5(PPP1R9B):c.79A>T (p.Ile27Phe) | not specified [RCV004196671] | uncertain significance | 17 | 50150435 | 50150435 | Human | | name |
| 329367365 | CV2456778 | single nucleotide variant | NM_032595.5(PPP1R9B):c.35C>G (p.Pro12Arg) | not specified [RCV004270753] | uncertain significance | 17 | 50150479 | 50150479 | Human | | name |
| 405286717 | CV3192242 | single nucleotide variant | NM_032595.5(PPP1R9B):c.333G>T (p.Leu111=) | PPP1R9B-related disorder [RCV003924144] | likely benign | 17 | 50150181 | 50150181 | Human | | name , trait , alternate_id |
| 405272743 | CV3197507 | single nucleotide variant | NM_032595.5(PPP1R9B):c.753C>T (p.Phe251=) | PPP1R9B-related disorder [RCV003901476] | likely benign | 17 | 50149761 | 50149761 | Human | | name , trait , alternate_id |
| 405274585 | CV3208932 | single nucleotide variant | NM_032595.5(PPP1R9B):c.774G>C (p.Pro258=) | PPP1R9B-related disorder [RCV003951712] | likely benign | 17 | 50149740 | 50149740 | Human | | name , trait , alternate_id |
| 597769272 | CV3587893 | single nucleotide variant | NM_032595.5(PPP1R9B):c.79A>G (p.Ile27Val) | not specified [RCV004850886] | uncertain significance | 17 | 50150435 | 50150435 | Human | | name |
| 598169967 | CV3907686 | single nucleotide variant | NM_032595.5(PPP1R9B):c.57C>A (p.His19Gln) | not specified [RCV005262954] | uncertain significance | 17 | 50150457 | 50150457 | Human | | name |
| 15165963 | CV715540 | single nucleotide variant | NM_032595.5(PPP1R9B):c.660G>A (p.Ser220=) | not provided [RCV000971066] | benign | 17 | 50149854 | 50149854 | Human | | name |
| 8644966 | CV104373 | single nucleotide variant | NM_032595.5(PPP1R9B):c.2358G>A (p.Ser786=) | not provided [RCV000084771] | not provided | 17 | 50135595 | 50135595 | Human | | name |
| 8644967 | CV104374 | single nucleotide variant | NM_032595.5(PPP1R9B):c.2238G>A (p.Ala746=) | not provided [RCV000084772] | not provided | 17 | 50136033 | 50136033 | Human | | name |
| 8644968 | CV104375 | single nucleotide variant | NM_032595.5(PPP1R9B):c.2199G>T (p.Leu733=) | not provided [RCV000084773] | not provided | 17 | 50136072 | 50136072 | Human | | name |
| 8644970 | CV104377 | single nucleotide variant | NM_032595.5(PPP1R9B):c.1590C>T (p.Thr530=) | not provided [RCV000084775] | not provided | 17 | 50143633 | 50143633 | Human | | name |
| 8644972 | CV104379 | single nucleotide variant | NM_032595.5(PPP1R9B):c.1509C>T (p.Ser503=) | not provided [RCV000084777] | not provided | 17 | 50143714 | 50143714 | Human | | name |
| 8644973 | CV104380 | single nucleotide variant | NM_032595.5(PPP1R9B):c.1332C>T (p.Ala444=) | not provided [RCV000084778] | not provided | 17 | 50149182 | 50149182 | Human | | name |
| 8644974 | CV104381 | single nucleotide variant | NM_032595.5(PPP1R9B):c.1137A>G (p.Val379=) | not provided [RCV000084779] | not provided | 17 | 50149377 | 50149377 | Human | | name |
| 8644975 | CV104382 | single nucleotide variant | NM_032595.5(PPP1R9B):c.1131G>A (p.Glu377=) | not provided [RCV000084780] | not provided | 17 | 50149383 | 50149383 | Human | | name |
| 8644977 | CV104384 | single nucleotide variant | NM_032595.5(PPP1R9B):c.1092G>A (p.Arg364=) | not provided [RCV000084782] | not provided | 17 | 50149422 | 50149422 | Human | | name |
| 8644978 | CV104385 | single nucleotide variant | NM_032595.5(PPP1R9B):c.1077A>G (p.Val359=) | not provided [RCV000084783] | not provided | 17 | 50149437 | 50149437 | Human | | name |
| 8644979 | CV104386 | single nucleotide variant | NM_032595.5(PPP1R9B):c.1074G>C (p.Ala358=) | not provided [RCV000084784] | not provided | 17 | 50149440 | 50149440 | Human | | name |
| 8644980 | CV104387 | single nucleotide variant | NM_032595.5(PPP1R9B):c.1071G>A (p.Ala357=) | not provided [RCV000084785] | not provided | 17 | 50149443 | 50149443 | Human | | name |
| 8644982 | CV104389 | single nucleotide variant | NM_032595.5(PPP1R9B):c.1047A>G (p.Gln349=) | not provided [RCV000084787] | not provided | 17 | 50149467 | 50149467 | Human | | name |
| 8644993 | CV104400 | single nucleotide variant | NM_032595.5(PPP1R9B):c.253C>T (p.Arg85Trp) | not provided [RCV000084798] | not provided | 17 | 50150261 | 50150261 | Human | | name |
| 155921140 | CV2212148 | single nucleotide variant | NM_032595.5(PPP1R9B):c.128A>T (p.Lys43Met) | not specified [RCV004089047] | uncertain significance | 17 | 50150386 | 50150386 | Human | | name |
| 329360993 | CV2463177 | single nucleotide variant | NM_032595.5(PPP1R9B):c.208C>T (p.Pro70Ser) | not specified [RCV004274958] | uncertain significance | 17 | 50150306 | 50150306 | Human | | name |
| 401729197 | CV2735143 | single nucleotide variant | NM_032595.5(PPP1R9B):c.209C>G (p.Pro70Arg) | not specified [RCV004333840] | uncertain significance | 17 | 50150305 | 50150305 | Human | | name |
| 401768043 | CV2735144 | single nucleotide variant | NM_032595.5(PPP1R9B):c.239T>C (p.Leu80Pro) | not specified [RCV004333841] | likely benign | 17 | 50150275 | 50150275 | Human | | name |
| 401768044 | CV2735145 | single nucleotide variant | NM_032595.5(PPP1R9B):c.241G>A (p.Ala81Thr) | not specified [RCV004333842] | likely benign | 17 | 50150273 | 50150273 | Human | | name |
| 401768047 | CV2735146 | single nucleotide variant | NM_032595.5(PPP1R9B):c.251C>T (p.Pro84Leu) | not specified [RCV004333843] | uncertain significance | 17 | 50150263 | 50150263 | Human | | name |
| 401768050 | CV2735147 | single nucleotide variant | NM_032595.5(PPP1R9B):c.259T>C (p.Ser87Pro) | not specified [RCV004333844] | likely benign | 17 | 50150255 | 50150255 | Human | | name |
| 401914398 | CV2811468 | single nucleotide variant | NM_032595.5(PPP1R9B):c.2346T>G (p.Val782=) | not provided [RCV003428325] | likely benign | 17 | 50135607 | 50135607 | Human | | name |
| 598202894 | CV3907689 | single nucleotide variant | NM_032595.5(PPP1R9B):c.176G>C (p.Ser59Thr) | not specified [RCV005269290] | uncertain significance | 17 | 50150338 | 50150338 | Human | | name |
| 15165960 | CV715539 | single nucleotide variant | NM_032595.5(PPP1R9B):c.1644C>A (p.Leu548=) | not provided [RCV000971065] | benign | 17 | 50141355 | 50141355 | Human | | name |
| 8636231 | CV91455 | single nucleotide variant | NM_032595.4(PPP1R9B):c.1644C>T (p.Leu548=) | Malignant melanoma [RCV000071553] | not provided | 17 | 50141355 | 50141355 | Human | | name |
| 8644983 | CV104390 | single nucleotide variant | NM_032595.5(PPP1R9B):c.815G>C (p.Cys272Ser) | not provided [RCV000084788] | not provided | 17 | 50149699 | 50149699 | Human | | name |
| 8644986 | CV104393 | single nucleotide variant | NM_032595.5(PPP1R9B):c.631C>T (p.Leu211Phe) | not provided [RCV000084791] | not provided | 17 | 50149883 | 50149883 | Human | | name |
| 8644989 | CV104396 | single nucleotide variant | NM_032595.5(PPP1R9B):c.506G>A (p.Arg169Gln) | not provided [RCV000084794] | not provided | 17 | 50150008 | 50150008 | Human | | name |
| 8644991 | CV104398 | single nucleotide variant | NM_032595.5(PPP1R9B):c.416A>C (p.His139Pro) | not provided [RCV000084796] | not provided | 17 | 50150098 | 50150098 | Human | | name |
| 152983372 | CV1678190 | single nucleotide variant | NM_032595.5(PPP1R9B):c.492G>C (p.Glu164Asp) | not provided [RCV004710438]|not specified [RCV002250347] | benign | 17 | 50150022 | 50150022 | Human | | name |
| 15162344 | CV704209 | variation | NM_032595.5(PPP1R9B):c.493_494= (p.Ala165=) | not provided [RCV000947837] | benign | 17 | 50150020 | 50150021 | Human | | name |
| 8644969 | CV104376 | single nucleotide variant | NM_032595.5(PPP1R9B):c.1916C>T (p.Pro639Leu) | not provided [RCV000084774] | not provided | 17 | 50139532 | 50139532 | Human | | name |
| 8644971 | CV104378 | single nucleotide variant | NM_032595.5(PPP1R9B):c.1582G>A (p.Val528Ile) | not provided [RCV000084776] | not provided | 17 | 50143641 | 50143641 | Human | | name |
| 8644976 | CV104383 | single nucleotide variant | NM_032595.5(PPP1R9B):c.1112C>T (p.Ala371Val) | not provided [RCV000084781] | not provided | 17 | 50149402 | 50149402 | Human | | name |
| 8644981 | CV104388 | single nucleotide variant | NM_032595.5(PPP1R9B):c.1059G>C (p.Glu353Asp) | not provided [RCV000084786] | not provided | 17 | 50149455 | 50149455 | Human | | name |
| 405263552 | CV3189739 | single nucleotide variant | NM_032595.5(PPP1R9B):c.1092G>T (p.Arg364Ser) | PPP1R9B-related disorder [RCV003896788] | likely benign | 17 | 50149422 | 50149422 | Human | | name , trait , alternate_id |
| 405283407 | CV3191362 | single nucleotide variant | NM_032595.5(PPP1R9B):c.1751G>A (p.Arg584Gln) | PPP1R9B-related disorder [RCV003921757] | likely benign | 17 | 50140208 | 50140208 | Human | | name , trait , alternate_id |
| 405271609 | CV3202921 | single nucleotide variant | NM_032595.5(PPP1R9B):c.2254G>A (p.Glu752Lys) | PPP1R9B-related disorder [RCV003913981] | uncertain significance | 17 | 50136017 | 50136017 | Human | | name , trait , alternate_id |
| 405274245 | CV3211600 | single nucleotide variant | NM_032595.5(PPP1R9B):c.1271C>T (p.Pro424Leu) | PPP1R9B-related disorder [RCV003951428] | likely benign | 17 | 50149243 | 50149243 | Human | | name , trait , alternate_id |
| 405291893 | CV3221131 | single nucleotide variant | NM_032595.5(PPP1R9B):c.1089G>C (p.Glu363Asp) | PPP1R9B-related disorder [RCV003964233] | benign | 17 | 50149425 | 50149425 | Human | | name , trait , alternate_id |
| 408366968 | CV3508244 | single nucleotide variant | NM_032595.5(PPP1R9B):c.1402G>T (p.Asp468Tyr) | PPP1R9B-related disorder [RCV004757656] | uncertain significance | 17 | 50145215 | 50145215 | Human | | name , trait , alternate_id |
| 13706147 | CV537289 | single nucleotide variant | NM_032595.5(PPP1R9B):c.2380A>C (p.Met794Leu) | not provided [RCV000658786] | uncertain significance | 17 | 50135573 | 50135573 | Human | | name |
| 405269031 | CV3199135 | duplication | NM_032595.5(PPP1R9B):c.472_473dup (p.Ala159fs) | PPP1R9B-related disorder [RCV003912237] | benign | 17 | 50150040 | 50150041 | Human | | name , trait , alternate_id |
| 405281151 | CV3190761 | insertion | NM_032595.5(PPP1R9B):c.490_491insGC (p.Glu164fs) | PPP1R9B-related disorder [RCV003907196] | benign | 17 | 50150023 | 50150024 | Human | | name , trait , alternate_id |
