| 329352126 | CV2452062 | single nucleotide variant | NM_001193308.2(SYTL1):c.80A>C (p.Glu27Ala) | not specified [RCV004278788] | uncertain significance | 1 | 27345414 | 27345414 | Human | | name |
| 405742712 | CV3334945 | single nucleotide variant | NM_001193308.2(SYTL1):c.28G>A (p.Glu10Lys) | not specified [RCV004465968] | uncertain significance | 1 | 27345362 | 27345362 | Human | | name |
| 329392614 | CV2471372 | single nucleotide variant | NM_001193308.2(SYTL1):c.185G>A (p.Arg62Gln) | not specified [RCV004280379] | uncertain significance | 1 | 27345519 | 27345519 | Human | | name |
| 405742707 | CV3334944 | single nucleotide variant | NM_001193308.2(SYTL1):c.262C>T (p.Arg88Cys) | not specified [RCV004465967] | uncertain significance | 1 | 27347491 | 27347491 | Human | | name |
| 597780744 | CV3619064 | single nucleotide variant | NM_001193308.2(SYTL1):c.121G>A (p.Glu41Lys) | not specified [RCV004873916] | uncertain significance | 1 | 27345455 | 27345455 | Human | | name |
| 598181282 | CV3923537 | single nucleotide variant | NM_001193308.2(SYTL1):c.233T>C (p.Ile78Thr) | not specified [RCV005286690] | uncertain significance | 1 | 27347462 | 27347462 | Human | | name |
| 156336754 | CV2228585 | single nucleotide variant | NM_001193308.2(SYTL1):c.686A>C (p.Asp229Ala) | not specified [RCV004092817] | uncertain significance | 1 | 27349704 | 27349704 | Human | | name |
| 155922160 | CV2284283 | single nucleotide variant | NM_001193308.2(SYTL1):c.586G>A (p.Glu196Lys) | not specified [RCV004146639] | uncertain significance | 1 | 27349451 | 27349451 | Human | | name |
| 155955838 | CV2303958 | single nucleotide variant | NM_001193308.2(SYTL1):c.539G>A (p.Gly180Asp) | not specified [RCV004168229] | uncertain significance | 1 | 27349404 | 27349404 | Human | | name |
| 156160212 | CV2322814 | single nucleotide variant | NM_001193308.2(SYTL1):c.616C>G (p.Arg206Gly) | not specified [RCV004182911] | uncertain significance | 1 | 27349481 | 27349481 | Human | | name |
| 156182492 | CV2338206 | single nucleotide variant | NM_001193308.2(SYTL1):c.788C>A (p.Ala263Glu) | not specified [RCV004186274] | uncertain significance | 1 | 27350012 | 27350012 | Human | | name |
| 156086642 | CV2340723 | single nucleotide variant | NM_001193308.2(SYTL1):c.883G>A (p.Ala295Thr) | not specified [RCV004190393] | uncertain significance | 1 | 27350107 | 27350107 | Human | | name |
| 155900828 | CV2345684 | single nucleotide variant | NM_001193308.2(SYTL1):c.685G>A (p.Asp229Asn) | not specified [RCV004205627] | uncertain significance | 1 | 27349703 | 27349703 | Human | | name |
| 156125704 | CV2350223 | single nucleotide variant | NM_001193308.2(SYTL1):c.893G>A (p.Arg298His) | not specified [RCV004200133] | uncertain significance | 1 | 27350117 | 27350117 | Human | | name |
| 156390111 | CV2373066 | single nucleotide variant | NM_001193308.2(SYTL1):c.446T>G (p.Leu149Arg) | not specified [RCV004217762] | uncertain significance | 1 | 27347999 | 27347999 | Human | | name |
| 329359295 | CV2450943 | single nucleotide variant | NM_001193308.2(SYTL1):c.383T>G (p.Val128Gly) | not specified [RCV004267835] | likely benign | 1 | 27347850 | 27347850 | Human | | name |
| 401744630 | CV2681092 | single nucleotide variant | NM_001193308.2(SYTL1):c.895C>A (p.Arg299Ser) | not specified [RCV004296151] | uncertain significance | 1 | 27350119 | 27350119 | Human | | name |
| 401726879 | CV2691882 | single nucleotide variant | NM_001193308.2(SYTL1):c.677C>G (p.Pro226Arg) | not specified [RCV004299622] | uncertain significance | 1 | 27349695 | 27349695 | Human | | name |
| 401736700 | CV2725181 | single nucleotide variant | NM_001193308.2(SYTL1):c.803G>C (p.Gly268Ala) | not specified [RCV004321708] | uncertain significance | 1 | 27350027 | 27350027 | Human | | name |
| 405742720 | CV3334946 | single nucleotide variant | NM_001193308.2(SYTL1):c.320G>A (p.Arg107His) | not specified [RCV004465969] | uncertain significance | 1 | 27347549 | 27347549 | Human | | name |
| 405742726 | CV3334947 | single nucleotide variant | NM_001193308.2(SYTL1):c.376G>A (p.Ala126Thr) | not specified [RCV004465970] | uncertain significance | 1 | 27347843 | 27347843 | Human | | name |
| 405742731 | CV3334948 | single nucleotide variant | NM_001193308.2(SYTL1):c.479C>T (p.Pro160Leu) | not specified [RCV004465971] | uncertain significance | 1 | 27349099 | 27349099 | Human | | name |
| 405742737 | CV3334949 | single nucleotide variant | NM_001193308.2(SYTL1):c.598G>T (p.Gly200Trp) | not specified [RCV004465972] | uncertain significance | 1 | 27349463 | 27349463 | Human | | name |
| 405742743 | CV3334950 | single nucleotide variant | NM_001193308.2(SYTL1):c.610G>A (p.Glu204Lys) | not specified [RCV004465973] | uncertain significance | 1 | 27349475 | 27349475 | Human | | name |
| 405742749 | CV3334951 | single nucleotide variant | NM_001193308.2(SYTL1):c.788C>T (p.Ala263Val) | not specified [RCV004465974] | uncertain significance | 1 | 27350012 | 27350012 | Human | | name |
| 405742754 | CV3334952 | single nucleotide variant | NM_001193308.2(SYTL1):c.967A>G (p.Lys323Glu) | not specified [RCV004465975] | uncertain significance | 1 | 27350447 | 27350447 | Human | | name |
| 407505965 | CV3478403 | single nucleotide variant | NM_001193308.2(SYTL1):c.697G>C (p.Asp233His) | not specified [RCV004670981] | uncertain significance | 1 | 27349715 | 27349715 | Human | | name |
| 597780715 | CV3619056 | single nucleotide variant | NM_001193308.2(SYTL1):c.565G>C (p.Glu189Gln) | not specified [RCV004873909] | uncertain significance | 1 | 27349430 | 27349430 | Human | | name |
| 597794692 | CV3619063 | single nucleotide variant | NM_001193308.2(SYTL1):c.539G>T (p.Gly180Val) | not specified [RCV004877940] | uncertain significance | 1 | 27349404 | 27349404 | Human | | name |
| 598264324 | CV3923538 | single nucleotide variant | NM_001193308.2(SYTL1):c.850C>A (p.Arg284Ser) | not specified [RCV005280747] | uncertain significance | 1 | 27350074 | 27350074 | Human | | name |
| 155940492 | CV2294086 | single nucleotide variant | NM_001193308.2(SYTL1):c.1601A>C (p.Lys534Thr) | not specified [RCV004149461] | uncertain significance | 1 | 27353764 | 27353764 | Human | | name |
| 156003127 | CV2347756 | single nucleotide variant | NM_001193308.2(SYTL1):c.1024G>A (p.Glu342Lys) | not specified [RCV004202722] | uncertain significance | 1 | 27350812 | 27350812 | Human | | name |
| 156132991 | CV2350222 | single nucleotide variant | NM_001193308.2(SYTL1):c.1406T>C (p.Leu469Pro) | not specified [RCV004200132] | uncertain significance | 1 | 27353345 | 27353345 | Human | | name |
| 155908958 | CV2354787 | single nucleotide variant | NM_001193308.2(SYTL1):c.1240G>A (p.Glu414Lys) | not specified [RCV004204772] | uncertain significance | 1 | 27351333 | 27351333 | Human | | name |
| 329374618 | CV2430961 | single nucleotide variant | NM_001193308.2(SYTL1):c.1322C>T (p.Ser441Phe) | not specified [RCV004248552] | uncertain significance | 1 | 27351534 | 27351534 | Human | | name |
| 329391956 | CV2445211 | single nucleotide variant | NM_001193308.2(SYTL1):c.1481T>G (p.Leu494Arg) | not specified [RCV004263845] | uncertain significance | 1 | 27353420 | 27353420 | Human | | name |
| 329354364 | CV2448045 | single nucleotide variant | NM_001193308.2(SYTL1):c.1039G>A (p.Val347Met) | not specified [RCV004263277] | uncertain significance | 1 | 27350827 | 27350827 | Human | | name |
| 329371758 | CV2454878 | single nucleotide variant | NM_001193308.2(SYTL1):c.1009T>C (p.Ser337Pro) | not specified [RCV004270378] | uncertain significance | 1 | 27350797 | 27350797 | Human | | name |
| 329394277 | CV2469789 | single nucleotide variant | NM_001193308.2(SYTL1):c.1282G>A (p.Val428Met) | not specified [RCV004285287] | uncertain significance | 1 | 27351494 | 27351494 | Human | | name |
| 405742689 | CV3334941 | single nucleotide variant | NM_001193308.2(SYTL1):c.1081A>C (p.Asn361His) | not specified [RCV004465964] | uncertain significance | 1 | 27350869 | 27350869 | Human | | name |
| 405743100 | CV3334942 | single nucleotide variant | NM_001193308.2(SYTL1):c.1636G>A (p.Glu546Lys) | not specified [RCV004465965] | uncertain significance | 1 | 27353799 | 27353799 | Human | | name |
| 405742701 | CV3334943 | single nucleotide variant | NM_001193308.2(SYTL1):c.1651C>T (p.Leu551Phe) | not specified [RCV004465966] | uncertain significance | 1 | 27353814 | 27353814 | Human | | name |
| 407505955 | CV3478400 | single nucleotide variant | NM_001193308.2(SYTL1):c.1463G>A (p.Arg488His) | not specified [RCV004670978] | uncertain significance | 1 | 27353402 | 27353402 | Human | | name |
| 407505958 | CV3478401 | single nucleotide variant | NM_001193308.2(SYTL1):c.1325T>G (p.Leu442Arg) | not specified [RCV004670979] | uncertain significance | 1 | 27351537 | 27351537 | Human | | name |
| 407505962 | CV3478402 | single nucleotide variant | NM_001193308.2(SYTL1):c.1402A>C (p.Ser468Arg) | not specified [RCV004670980] | uncertain significance | 1 | 27353341 | 27353341 | Human | | name |
| 597780721 | CV3619057 | single nucleotide variant | NM_001193308.2(SYTL1):c.1651C>G (p.Leu551Val) | not specified [RCV004873910] | uncertain significance | 1 | 27353814 | 27353814 | Human | | name |
| 597780733 | CV3619060 | single nucleotide variant | NM_001193308.2(SYTL1):c.1322C>A (p.Ser441Tyr) | not specified [RCV004873913] | uncertain significance | 1 | 27351534 | 27351534 | Human | | name |
| 597780736 | CV3619061 | single nucleotide variant | NM_001193308.2(SYTL1):c.1514G>A (p.Arg505His) | not specified [RCV004873914] | uncertain significance | 1 | 27353453 | 27353453 | Human | | name |
| 597780740 | CV3619062 | single nucleotide variant | NM_001193308.2(SYTL1):c.1012G>A (p.Val338Ile) | not specified [RCV004873915] | uncertain significance | 1 | 27350800 | 27350800 | Human | | name |
| 597780748 | CV3619065 | single nucleotide variant | NM_001193308.2(SYTL1):c.1660C>T (p.Leu554Phe) | not specified [RCV004873917] | uncertain significance | 1 | 27353823 | 27353823 | Human | | name |
| 597780752 | CV3619066 | single nucleotide variant | NM_001193308.2(SYTL1):c.1307C>G (p.Pro436Arg) | not specified [RCV004873918] | uncertain significance | 1 | 27351519 | 27351519 | Human | | name |
| 598264309 | CV3923532 | single nucleotide variant | NM_001193308.2(SYTL1):c.1460T>C (p.Leu487Pro) | not specified [RCV005280745] | uncertain significance | 1 | 27353399 | 27353399 | Human | | name |
| 598181267 | CV3923533 | single nucleotide variant | NM_001193308.2(SYTL1):c.1235G>A (p.Gly412Asp) | not specified [RCV005286687] | uncertain significance | 1 | 27351328 | 27351328 | Human | | name |
| 598181272 | CV3923534 | single nucleotide variant | NM_001193308.2(SYTL1):c.1348G>A (p.Val450Met) | not specified [RCV005286688] | uncertain significance | 1 | 27353287 | 27353287 | Human | | name |
| 598264316 | CV3923535 | single nucleotide variant | NM_001193308.2(SYTL1):c.1626G>C (p.Glu542Asp) | not specified [RCV005280746] | uncertain significance | 1 | 27353789 | 27353789 | Human | | name |
