Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32339505_32339581delinsTACTTAATACTTATTAAGTATTACA2499222187BRCA2c.5150_5226delinsTACTTAATACTTATTAAGTATTA (p.Glu1717ValfsTer6)
c.4781_4857delinsTACTTAATACTTATTAAGTATTA (p.Glu1594ValfsTer6)
n.5150_5226delinsTACTTAATACTTATTAAGTATTA
ClinVar dbSNP
13g.32339554_32340264delCA2580087342BRCA2c.5199_5909del (p.Glu1734_Ser1970del)
c.4830_5540del (p.Glu1611_Ser1847del)
n.5199_5909del
ClinVar
13g.32339555G>ACA021678BRCA2c.5200G>A (p.Glu1734Lys)
c.4831G>A (p.Glu1611Lys)
n.5200G>A
ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32339555G>CCA387784590BRCA2c.5200G>C (p.Glu1734Gln)
c.4831G>C (p.Glu1611Gln)
n.5200G>C
ClinVar dbSNP
13g.32339555G=CA2082820151BRCA2c.5200G= (p.Glu1734=)
c.4831G= (p.Glu1611=)
n.5200G=
13g.32339555G>TCA10586538BRCA2c.5200G>T (p.Glu1734Ter)
c.4831G>T (p.Glu1611Ter)
n.5200G>T
ClinVar dbSNP gnomAD v4
13g.32339555dupCA658683841BRCA2c.5200dup (p.Glu1734GlyfsTer9)
c.4831dup (p.Glu1611GlyfsTer9)
n.5200dup
ClinVar dbSNP
13g.32339555_32339560delinsGAAAAACA2082820160BRCA2c.5200_5205delinsGAAAAA (p.Glu1734=)
c.4831_4836delinsGAAAAA (p.Glu1611=)
n.5200_5205delinsGAAAAA
13g.32339556A=CA2082820172BRCA2c.5201A= (p.Glu1734=)
c.4832A= (p.Glu1611=)
n.5201A=
13g.32339556A>CCA387784591BRCA2c.5201A>C (p.Glu1734Ala)
c.4832A>C (p.Glu1611Ala)
n.5201A>C
dbSNP
13g.32339556A>GCA387784592BRCA2c.5201A>G (p.Glu1734Gly)
c.4832A>G (p.Glu1611Gly)
n.5201A>G
13g.32339556A>TCA387784593BRCA2c.5201A>T (p.Glu1734Val)
c.4832A>T (p.Glu1611Val)
n.5201A>T
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32339556_32339560delinsGAAAAGCA645509350BRCA2c.5201_5205delinsGAAAAG (p.Glu1734GlyfsTer9)
c.4832_4836delinsGAAAAG (p.Glu1611GlyfsTer9)
n.5201_5205delinsGAAAAG
ClinVar dbSNP
13g.32339560dupCA658656382BRCA2c.5205dup (p.Gln1736ThrfsTer7)
c.4836dup (p.Gln1613ThrfsTer7)
n.5205dup
ClinVar dbSNP
13g.32339560delCA10589296BRCA2c.5205del (p.Lys1735AsnfsTer6)
c.4836del (p.Lys1612AsnfsTer6)
n.5205del
ClinVar dbSNP
13g.32339557A=CA2082820195BRCA2c.5202A= (p.Glu1734=)
c.4833A= (p.Glu1611=)
n.5202A=
13g.32339557A>CCA387784594BRCA2c.5202A>C (p.Glu1734Asp)
c.4833A>C (p.Glu1611Asp)
n.5202A>C
ClinVar dbSNP gnomAD v4
13g.32339557A>GCA483438370BRCA2c.5202A>G (p.Glu1734=)
c.4833A>G (p.Glu1611=)
n.5202A>G
13g.32339557A>TCA387784595BRCA2c.5202A>T (p.Glu1734Asp)
c.4833A>T (p.Glu1611Asp)
n.5202A>T
gnomAD v4
13g.32339557_32339561delinsAAAACCA2082820189BRCA2c.5202_5206delinsAAAAC (p.Glu1734=)
c.4833_4837delinsAAAAC (p.Glu1611=)
n.5202_5206delinsAAAAC
13g.32339558A>CCA387784596BRCA2c.5203A>C (p.Lys1735Gln)
c.4834A>C (p.Lys1612Gln)
n.5203A>C
13g.32339558A>GCA387784598BRCA2c.5203A>G (p.Lys1735Glu)
c.4834A>G (p.Lys1612Glu)
n.5203A>G
dbSNP
13g.32339558A>TCA387784597BRCA2c.5203A>T (p.Lys1735Ter)
c.4834A>T (p.Lys1612Ter)
n.5203A>T
dbSNP
13g.32339560_32339563delCA10589295BRCA2c.5205_5208del (p.Gln1736IlefsTer4)
c.4836_4839del (p.Gln1613IlefsTer4)
n.5205_5208del
ClinVar dbSNP
13g.32339559A>CCA387784599BRCA2c.5204A>C (p.Lys1735Thr)
c.4835A>C (p.Lys1612Thr)
n.5204A>C
13g.32339559A>GCA387784600BRCA2c.5204A>G (p.Lys1735Arg)
c.4835A>G (p.Lys1612Arg)
n.5204A>G
dbSNP
13g.32339559A>TCA387784601BRCA2c.5204A>T (p.Lys1735Ile)
c.4835A>T (p.Lys1612Ile)
n.5204A>T
dbSNP
13g.32339560A=CA2082820212BRCA2c.5205A= (p.Lys1735=)
c.4836A= (p.Lys1612=)
n.5205A=
13g.32339560A>CCA387784602BRCA2c.5205A>C (p.Lys1735Asn)
c.4836A>C (p.Lys1612Asn)
n.5205A>C
dbSNP
13g.32339560A>GCA483438373BRCA2c.5205A>G (p.Lys1735=)
c.4836A>G (p.Lys1612=)
n.5205A>G
ClinVar dbSNP gnomAD v4
13g.32339560A>TCA387784603BRCA2c.5205A>T (p.Lys1735Asn)
c.4836A>T (p.Lys1612Asn)
n.5205A>T
ClinVar dbSNP
13g.32339561_32339562delCA2697551795BRCA2c.5206_5207del (p.Gln1736ArgfsTer6)
c.4837_4838del (p.Gln1613ArgfsTer6)
n.5206_5207del
13g.32339561C>ACA387784604BRCA2c.5206C>A (p.Gln1736Lys)
c.4837C>A (p.Gln1613Lys)
n.5206C>A
dbSNP
13g.32339561C=CA2082820226BRCA2c.5206C= (p.Gln1736=)
c.4837C= (p.Gln1613=)
n.5206C=
13g.32339561C>GCA387784605BRCA2c.5206C>G (p.Gln1736Glu)
c.4837C>G (p.Gln1613Glu)
n.5206C>G
ClinVar dbSNP gnomAD v4
13g.32339561C>TCA10575921BRCA2c.5206C>T (p.Gln1736Ter)
c.4837C>T (p.Gln1613Ter)
n.5206C>T
ClinVar dbSNP
13g.32339561_32339562delinsCACA2082820224BRCA2c.5206_5207delinsCA (p.Gln1736=)
c.4837_4838delinsCA (p.Gln1613=)
n.5206_5207delinsCA
13g.32339561_32339563delinsCAACA2082820221BRCA2c.5206_5208delinsCAA (p.Gln1736=)
c.4837_4839delinsCAA (p.Gln1613=)
n.5206_5208delinsCAA
13g.32339562A=CA2082820256BRCA2c.5207A= (p.Gln1736=)
c.4838A= (p.Gln1613=)
n.5207A=
13g.32339562A>CCA387784608BRCA2c.5207A>C (p.Gln1736Pro)
c.4838A>C (p.Gln1613Pro)
n.5207A>C
dbSNP
13g.32339562A>GCA387784607BRCA2c.5207A>G (p.Gln1736Arg)
c.4838A>G (p.Gln1613Arg)
n.5207A>G
ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32339562A>TCA387784606BRCA2c.5207A>T (p.Gln1736Leu)
c.4838A>T (p.Gln1613Leu)
n.5207A>T
dbSNP
13g.32339562_32339563delCA021686BRCA2c.5207_5208del (p.Gln1736ArgfsTer6)
c.4838_4839del (p.Gln1613ArgfsTer6)
n.5207_5208del
ClinVar dbSNP
13g.32339563delCA021689BRCA2c.5208del (p.Asp1737IlefsTer4)
c.4839del (p.Asp1614IlefsTer4)
n.5208del
ClinVar dbSNP
13g.32339564_32339628dupCA915948485BRCA2c.5209_5273dup (p.Asn1758LysfsTer5)
c.4840_4904dup (p.Asn1635LysfsTer5)
n.5209_5273dup
ClinVar dbSNP
13g.32339563A=CA2082820271BRCA2c.5208A= (p.Gln1736=)
c.4839A= (p.Gln1613=)
n.5208A=
13g.32339563A>CCA387784609BRCA2c.5208A>C (p.Gln1736His)
c.4839A>C (p.Gln1613His)
n.5208A>C
13g.32339563A>GCA483438377BRCA2c.5208A>G (p.Gln1736=)
c.4839A>G (p.Gln1613=)
n.5208A>G
ClinVar dbSNP gnomAD v4
13g.32339563A>TCA387784610BRCA2c.5208A>T (p.Gln1736His)
c.4839A>T (p.Gln1613His)
n.5208A>T
dbSNP
13g.32339564delCA2697551796BRCA2c.5209del (p.Asp1737IlefsTer4)
c.4840del (p.Asp1614IlefsTer4)
n.5209del

Number of alleles fetched