ClinVar Miner

List of variants in gene VPS13B reported as likely benign for History of neurodevelopmental disorder

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 52
Download table as spreadsheet
HGVS dbSNP
NM_015243.2(VPS13B):c.1041A>G (p.Ser347=) rs149176010
NM_015243.2(VPS13B):c.1440C>T (p.Phe480=) rs141324814
NM_015243.2(VPS13B):c.1536A>G (p.Glu512=) rs145969836
NM_015243.2(VPS13B):c.1551A>C (p.Ser517=)
NM_015243.2(VPS13B):c.1782T>C (p.Ile594=) rs145648860
NM_015243.2(VPS13B):c.1832G>A (p.Arg611Lys) rs61754109
NM_015243.2(VPS13B):c.711T>C (p.Arg237=)
NM_015243.2(VPS13B):c.723A>G (p.Thr241=)
NM_015243.2(VPS13B):c.90A>G (p.Leu30=)
NM_017890.4(VPS13B):c.10127A>T (p.Asn3376Ile) rs111353525
NM_017890.4(VPS13B):c.10315T>C (p.Leu3439=) rs145279584
NM_017890.4(VPS13B):c.10920C>T (p.Ala3640=) rs781485612
NM_017890.4(VPS13B):c.10956G>A (p.Gly3652=)
NM_017890.4(VPS13B):c.10980T>C (p.Pro3660=) rs61754107
NM_017890.4(VPS13B):c.11007C>T (p.Asn3669=) rs745337140
NM_017890.4(VPS13B):c.11013C>T (p.Val3671=) rs758028194
NM_017890.4(VPS13B):c.11049C>G (p.Thr3683=)
NM_017890.4(VPS13B):c.11121T>A (p.Gly3707=) rs1178600682
NM_017890.4(VPS13B):c.11256A>G (p.Arg3752=) rs138667007
NM_017890.4(VPS13B):c.11388G>A (p.Ser3796=)
NM_017890.4(VPS13B):c.11688C>T (p.Phe3896=) rs139436386
NM_017890.4(VPS13B):c.2760A>G (p.Leu920=) rs138661755
NM_017890.4(VPS13B):c.3075G>A (p.Thr1025=) rs141637316
NM_017890.4(VPS13B):c.3204A>G (p.Thr1068=)
NM_017890.4(VPS13B):c.3386A>G (p.Lys1129Arg) rs61759485
NM_017890.4(VPS13B):c.3413C>T (p.Pro1138Leu) rs35342235
NM_017890.4(VPS13B):c.3465G>A (p.Thr1155=)
NM_017890.4(VPS13B):c.3516A>G (p.Thr1172=) rs118158347
NM_017890.4(VPS13B):c.3621C>T (p.Leu1207=)
NM_017890.4(VPS13B):c.3866C>G (p.Thr1289Ser) rs145569846
NM_017890.4(VPS13B):c.4281C>T (p.Cys1427=) rs1563767252
NM_017890.4(VPS13B):c.5064C>A (p.Pro1688=)
NM_017890.4(VPS13B):c.5544A>G (p.Leu1848=)
NM_017890.4(VPS13B):c.5577G>A (p.Ser1859=)
NM_017890.4(VPS13B):c.5681C>T (p.Thr1894Met) rs117148013
NM_017890.4(VPS13B):c.5682G>A (p.Thr1894=) rs368851580
NM_017890.4(VPS13B):c.6491A>G (p.Asn2164Ser) rs142248228
NM_017890.4(VPS13B):c.7005G>A (p.Gly2335=)
NM_017890.4(VPS13B):c.7227G>A (p.Pro2409=) rs61753725
NM_017890.4(VPS13B):c.7413T>C (p.Phe2471=) rs150771329
NM_017890.4(VPS13B):c.7753G>A (p.Glu2585Lys) rs111751379
NM_017890.4(VPS13B):c.7783G>A (p.Asp2595Asn) rs140179844
NM_017890.4(VPS13B):c.7791A>G (p.Val2597=)
NM_017890.4(VPS13B):c.7941G>A (p.Val2647=)
NM_017890.4(VPS13B):c.8246A>G (p.Tyr2749Cys) rs138453594
NM_017890.4(VPS13B):c.8917A>G (p.Ile2973Val)
NM_017890.4(VPS13B):c.8978A>G (p.Asn2993Ser) rs28940272
NM_017890.4(VPS13B):c.9444C>T (p.Cys3148=) rs745668942
NM_017890.4(VPS13B):c.9667C>T (p.Arg3223Trp) rs149842139
NM_017890.4(VPS13B):c.9858C>T (p.Ser3286=)
NM_017890.4(VPS13B):c.9943T>C (p.Leu3315=) rs1391149548
NM_017890.4(VPS13B):c.9996C>T (p.Asp3332=)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.