Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.40080483C>ACA263521PPT1c.*377G>T (n.*377G>T)
c.538G>T (p.Val180Leu)
c.541G>T (p.Val181Leu)
c.232G>T (p.Val78Leu)
c.310G>T (p.Val104Leu)
c.-117G>T (n.-117G>T)
c.*164G>T (n.*164G>T)
c.519G>T
n.778G>T
c.149-3570G>T
c.628G>T (p.Val210Leu)
c.*393G>T (n.*393G>T)
c.129G>T (p.Ser43=)
c.226G>T (p.Val76Leu)
c.316G>T (p.Val106Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.40080483C>TCA274047PPT1c.*377G>A (n.*377G>A)
c.538G>A (p.Val180Met)
c.541G>A (p.Val181Met)
c.232G>A (p.Val78Met)
c.310G>A (p.Val104Met)
c.-117G>A (n.-117G>A)
c.*164G>A (n.*164G>A)
c.519G>A
n.778G>A
c.149-3570G>A
c.628G>A (p.Val210Met)
c.*393G>A (n.*393G>A)
c.129G>A (p.Ser43=)
c.226G>A (p.Val76Met)
c.316G>A (p.Val106Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.40080483C>GCA339847926PPT1c.*377G>C (n.*377G>C)
c.538G>C (p.Val180Leu)
c.541G>C (p.Val181Leu)
c.232G>C (p.Val78Leu)
c.310G>C (p.Val104Leu)
c.-117G>C (n.-117G>C)
c.*164G>C (n.*164G>C)
c.519G>C
n.778G>C
c.149-3570G>C
c.628G>C (p.Val210Leu)
c.*393G>C (n.*393G>C)
c.129G>C (p.Ser43=)
c.226G>C (p.Val76Leu)
c.316G>C (p.Val106Leu)
ClinVar dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched