Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.28768203G>ACA123555FOXG1c.924G>A (p.Trp308Ter)
ClinVar dbSNP
14g.28768203G>CCA389476153FOXG1c.924G>C (p.Trp308Cys)
COSMIC
14g.28768203G=CA2126000321FOXG1c.924G= (p.Trp308=)
14g.28768203G>TCA389476152FOXG1c.924G>T (p.Trp308Cys)
14g.28768204C>ACA389476154FOXG1c.925C>A (p.Pro309Thr)
14g.28768204C=CA2126000322FOXG1c.925C= (p.Pro309=)
14g.28768204C>GCA389476155FOXG1c.925C>G (p.Pro309Ala)
14g.28768204C>TCA389476156FOXG1c.925C>T (p.Pro309Ser)
dbSNP gnomAD v2 gnomAD v4
14g.28768205C>ACA389476157FOXG1c.926C>A (p.Pro309His)
14g.28768205C=CA2126000323FOXG1c.926C= (p.Pro309=)
14g.28768205C>GCA258396587FOXG1c.926C>G (p.Pro309Arg)
dbSNP
14g.28768205C>TCA389476158FOXG1c.926C>T (p.Pro309Leu)
14g.28768206C>ACA486098300FOXG1c.927C>A (p.Pro309=)
gnomAD v4
14g.28768206C=CA2126000324FOXG1c.927C= (p.Pro309=)
14g.28768206C>GCA486098299FOXG1c.927C>G (p.Pro309=)
14g.28768206C>TCA486098298FOXG1c.927C>T (p.Pro309=)
dbSNP gnomAD v3 gnomAD v4
14g.28768207A>CCA389476159FOXG1c.928A>C (p.Met310Leu)
gnomAD v4
14g.28768207A>GCA389476160FOXG1c.928A>G (p.Met310Val)
14g.28768207A>TCA389476161FOXG1c.928A>T (p.Met310Leu)
14g.28768208T>ACA389476163FOXG1c.929T>A (p.Met310Lys)
14g.28768208T>CCA389476164FOXG1c.929T>C (p.Met310Thr)
14g.28768208T>GCA389476162FOXG1c.929T>G (p.Met310Arg)
14g.28768209G>ACA389476165FOXG1c.930G>A (p.Met310Ile)
14g.28768209G>CCA389476166FOXG1c.930G>C (p.Met310Ile)
14g.28768209G>TCA389476167FOXG1c.930G>T (p.Met310Ile)
14g.28768210T>ACA389476168FOXG1c.931T>A (p.Ser311Thr)
14g.28768210T>CCA389476169FOXG1c.931T>C (p.Ser311Pro)
14g.28768210T>GCA389476170FOXG1c.931T>G (p.Ser311Ala)
14g.28768211C>ACA389476171FOXG1c.932C>A (p.Ser311Ter)
dbSNP
14g.28768211C>GCA389476172FOXG1c.932C>G (p.Ser311Trp)
14g.28768211C>TCA389476173FOXG1c.932C>T (p.Ser311Leu)
14g.28768212G>ACA486098302FOXG1c.933G>A (p.Ser311=)
ClinVar
14g.28768212G>CCA486098304FOXG1c.933G>C (p.Ser311=)
gnomAD v4
14g.28768212G=CA2126000325FOXG1c.933G= (p.Ser311=)
14g.28768212G>TCA486098303FOXG1c.933G>T (p.Ser311=)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.28768213C>ACA389476174FOXG1c.934C>A (p.Pro312Thr)
14g.28768213C>GCA389476175FOXG1c.934C>G (p.Pro312Ala)
14g.28768213C>TCA389476176FOXG1c.934C>T (p.Pro312Ser)
gnomAD v4
14g.28768214C>ACA389476179FOXG1c.935C>A (p.Pro312His)
14g.28768214C>GCA389476177FOXG1c.935C>G (p.Pro312Arg)
14g.28768214C>TCA389476178FOXG1c.935C>T (p.Pro312Leu)
14g.28768215C>ACA486098308FOXG1c.936C>A (p.Pro312=)
14g.28768215C=CA2126000326FOXG1c.936C= (p.Pro312=)
14g.28768215C>GCA486098309FOXG1c.936C>G (p.Pro312=)
gnomAD v4
14g.28768215C>TCA486098310FOXG1c.936C>T (p.Pro312=)
ClinVar dbSNP gnomAD v4
14g.28768216T>ACA389476180FOXG1c.937T>A (p.Phe313Ile)
14g.28768216T>CCA389476181FOXG1c.937T>C (p.Phe313Leu)
gnomAD v4
14g.28768216T>GCA389476182FOXG1c.937T>G (p.Phe313Val)
14g.28768217T>ACA389476183FOXG1c.938T>A (p.Phe313Tyr)
14g.28768217T>CCA389476184FOXG1c.938T>C (p.Phe313Ser)

Number of alleles fetched