44300295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118930352-A-G

44301149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118929504-A-G

44301324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118929272-A-G

44301511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118929070-T-C

44302700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118928255-G-A

44302703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118928252-A-G

44302782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118928174-A-G

44302843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118928113-C-T

44302926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118928028-T-C

http://identifiers.org/hco/5/GRCh38#44303080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118927873-A-C

http://identifiers.org/hco/5/GRCh38#44303332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118927610-A-C

44303415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118927518-C-G

44303415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118927518-C-T

44303597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118927352-A-G

44303626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118927323-A-G

44303866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118927086-G-A

44303866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118927086-G-C

44303898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118927047-G-A

44303898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118927047-G-T

44303937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118927006-G-A

http://identifiers.org/hco/5/GRCh38#44304124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118926829-C-A

44304124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118926829-C-T

44304247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118926705-A-G

44304601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118926267-G-A

44304601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118926267-G-T

44304607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118926261-G-T

44304774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118926078-G-A

44304774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118926078-G-C

44304774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118926078-G-T

44304917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118925928-A-G

44304917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118925928-A-T

44304933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118925912-A-G

44304971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 3 prime UTR variant
orthologous variants: 118925874-T-C

44305089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: missense variant
orthologous variants: 118925756-A-G

44305255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118925592-A-T

44305259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118925588-A-T

44305330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118925513-A-G

44305566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118925268-G-A

44306767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118923604-T-C

44306777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118923594-T-C

44306905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118923478-A-T

44307556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118921658-G-A

44307578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118921636-G-A

44307578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118921636-G-T

44308062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118921270-G-T

44308481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118920822-T-A

44308481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118920822-T-G

44308884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118919790-C-T

44308905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118919772-A-G

44308943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118919734-G-A

44308946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118919731-C-T

http://identifiers.org/hco/5/GRCh38#44309590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118918983-A-C

44310039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118918517-A-G

http://identifiers.org/hco/5/GRCh38#44310280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118918277-C-A

44310354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118918218-T-C

44310434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: missense variant
orthologous variants: 118918136-T-C

44310471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: missense variant
orthologous variants: 118918099-T-A

44310471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: missense variant
orthologous variants: 118918099-T-C

44310499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: synonymous variant
orthologous variants: 118918071-T-G

44310565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118918004-A-T

http://identifiers.org/hco/5/GRCh38#44310602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118917966-A-C

44310602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118917966-A-T

44310607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118917961-A-T

44310612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118917956-G-T

44310880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118917705-T-G

44310946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118917632-A-G

44311097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118917475-C-T

http://identifiers.org/hco/5/GRCh38#44311272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118917331-A-C

44311371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118917233-A-G

44311533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118917078-A-G

http://identifiers.org/hco/5/GRCh38#44311651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118916972-C-A

44311844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118916769-A-G

44312419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118915519-C-T

44312640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118915328-G-C

44312645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118915323-T-C

http://identifiers.org/hco/5/GRCh38#44312977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118914916-C-A

44312977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118914916-C-T

44313030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118914865-C-G

44313152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118914632-T-C

44313429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118914164-T-C

http://identifiers.org/hco/5/GRCh38#44313567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118914034-C-A

http://identifiers.org/hco/5/GRCh38#44315636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118913949-A-C

44315636-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118913949-A-T

44315699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118913888-A-G

44315760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118913819-C-T

http://identifiers.org/hco/5/GRCh38#44315793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118913795-C-A

44315793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118913795-C-T

44316335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118911722-G-A

44316336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118911721-T-A

44316351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118911706-T-A

44316351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118911706-T-C

44316399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118911660-A-G

http://identifiers.org/hco/5/GRCh38#44316422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118911640-A-C

44316490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118911575-T-C

44316803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118911270-T-C

44317080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118910798-G-T

http://identifiers.org/hco/5/GRCh38#44317151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118910730-C-A

44317151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118910730-C-T

44318524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118908723-G-C

44318524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118908723-G-T

44318833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118908438-A-G

44318992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118908223-C-T

44318996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118908220-T-C

44319096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118908109-C-T

44319308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118907867-C-T

44319608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118907573-C-T

44319768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118907474-A-G

44319793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118907450-G-A

44323216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118907246-G-A

44323220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118907242-G-A

44323226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118907236-C-T

http://identifiers.org/hco/5/GRCh38#44323497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118907011-C-A

44323497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118907011-C-T

44323756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118906764-T-A

44323768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118906752-C-T

44323966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118906553-A-T

44323997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118906490-C-G

44324007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118906466-C-T

44324189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118906280-G-T

44324267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118906197-A-T

44324307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118906155-T-C

http://identifiers.org/hco/5/GRCh38#44324318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118906143-C-A

44324503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118905901-C-T

44324688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118905702-T-C

44324921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118905212-T-C

44324948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118905188-G-A

44325022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118905098-A-T

44325898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118905034-A-G

http://identifiers.org/hco/5/GRCh38#44325944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118904988-C-A

44325944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118904988-C-G

44325944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118904988-C-T

44326000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118904932-T-C

http://identifiers.org/hco/5/GRCh38#44326063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118904853-A-C

44326173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118904693-A-T

44326338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118904540-T-C

44326372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118904511-T-A

44326778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118904402-A-G

44326896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118904284-G-A

44327000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118904180-G-A

44327005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118904175-G-T

44327013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118904167-A-G

44327014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118904166-G-A

44327015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118904165-T-C

44327055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118904134-T-C

44327105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118904104-T-A

44327245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118903978-G-A

44327628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118903543-T-C

44327992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118903178-T-C

44328164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118903052-A-G

44328441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118902823-A-T

http://identifiers.org/hco/5/GRCh38#44329012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118902797-C-A

44329123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118902690-G-A

44329605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118902528-A-G

44329878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118902299-C-T

44330200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118902013-G-A

44330224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118901995-C-T

44330234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118901985-A-G

44330518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118901709-A-T

44331062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118901171-G-C

44331378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118900858-A-G

44331611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118900688-G-A

44331611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118900688-G-C

44331611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118900688-G-T

44331980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118900323-G-A

44332275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118900010-C-T

44332625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118899658-T-C

http://identifiers.org/hco/5/GRCh38#44336164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118898674-A-C

44336199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118898621-T-A

44336229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118898591-T-A

http://identifiers.org/hco/5/GRCh38#44336243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118898556-C-A

44336523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118898104-T-C

44336706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118897924-T-A

44336933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118897690-C-T

44336988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118897633-A-G

44337277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118897347-T-C

44337332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118897293-C-G

44338305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118896892-T-C

44338305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118896892-T-G

44338595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118896595-A-G

44338748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118896444-G-A

44338825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118896367-G-C

44338891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118896329-C-G

44339710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118895643-C-T

http://identifiers.org/hco/5/GRCh38#44339865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118895491-C-A

44339865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118895491-C-T

44340340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118894857-T-C

http://identifiers.org/hco/5/GRCh38#44340419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118894781-C-A

44340419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118894781-C-T

44340661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118894553-T-A

44342708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118893962-T-G

44342709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118893961-G-A

44342797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118893888-T-C

44343803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118893205-T-C

http://identifiers.org/hco/5/GRCh38#44344121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118892906-C-A

44344295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118892727-G-A

44344388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118892628-T-A

44344703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118892321-T-C

44345048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118892004-A-T

44345050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118892002-G-A

44345055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118891997-T-C

44345241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118891354-A-G

44345284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118891310-T-C

44345439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118891167-G-A

44345439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118891167-G-T

44345458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118891148-A-G

http://identifiers.org/hco/5/GRCh38#44345477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118891129-C-A

44345498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118891106-G-T

44345570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118891032-C-T

44345666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118890934-G-T

44345879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118890760-T-C

44346037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118890607-C-T

44346110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118890534-G-T

44346217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118890435-G-T

44346634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118890014-T-A

44346802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118889871-A-G

44346836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118889837-T-C

http://identifiers.org/hco/5/GRCh38#44346923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118889751-C-A

44347080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118889627-C-T

44347095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118889612-A-G

44347610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118889341-G-A

44347641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118889323-T-C

44347670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118889295-C-T

44347737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118889226-T-G

44347903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118888936-G-T

44348142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118888011-T-A

44348568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118887668-C-T

44349003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118887286-C-T

44349148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118887167-T-A

44349225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118887156-G-C

44349225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118887156-G-T

http://identifiers.org/hco/5/GRCh38#44349426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118887013-A-C

44349426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118887013-A-G

44349426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118887013-A-T

http://identifiers.org/hco/5/GRCh38#44349450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118886977-A-C

44349702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118886727-G-C

44349820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118886622-T-C

44350185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118886240-G-T

44350649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118885930-G-A

44350649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118885930-G-T

44350786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118885822-T-G

44350852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118885732-T-A

44350854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118885730-T-C

44350941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118885652-C-T

44351525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118885167-G-A

44351536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118885156-G-A

44351536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118885156-G-C

44351756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118884809-G-T

44351876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118884695-T-C

http://identifiers.org/hco/5/GRCh38#44354567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118883463-C-A

44354959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118883076-T-A

44354988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118883043-C-T

44355061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118882964-A-G

44355262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118882767-G-A

44355324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118882720-C-T

http://identifiers.org/hco/5/GRCh38#44355345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118882699-A-C

44355345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118882699-A-G

44355655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118882472-T-C

44355753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118882384-G-A

44355819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118882314-T-C

44355948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118882186-T-C

44355948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118882186-T-G

44356729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118881422-A-G

44357271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118880901-T-C

44357271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118880901-T-G

44357479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118880693-T-C

44357986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118880260-G-A

44358033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118880216-G-A

44358033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118880216-G-C

44358106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118880141-T-C

44358264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118880001-T-C

44358470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118879786-G-A

44358689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118879568-C-T

44359575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118878709-A-T

44359779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118878594-G-C

44359857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118878549-C-T

44359964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118878458-C-T

44360019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118878422-G-T

44360325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118878165-T-G

44360466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118878019-A-T

44360624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118877862-C-T

44360988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118877402-T-C

44361071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118877319-G-T

http://identifiers.org/hco/5/GRCh38#44361214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118877187-A-C

http://identifiers.org/hco/5/GRCh38#44361471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118876931-C-A

44361656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118876746-T-C

44362315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118875812-C-T

44362350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118875788-C-T

44362352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118875786-C-T

44362411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118875729-C-T

44362421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118875719-A-G

44362726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118875866-G-A

44362747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118875845-A-G

44362815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118875788-C-G

44362815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118875788-C-T

44362817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118875786-C-G

44362919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118875691-T-C

44363007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118875596-C-T

44363288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118875306-T-C

44363433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118875167-T-C

http://identifiers.org/hco/5/GRCh38#44363607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118874975-A-C

44363822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118874764-T-C

http://identifiers.org/hco/5/GRCh38#44365056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118873813-A-C

44365081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118873788-C-T

44365343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118873544-T-A

44365461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron_variant, undefined
orthologous variants: 118873444-A-T

44365664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118873239-C-T

44365743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118873179-T-C

44365750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118873172-T-C

44365777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118873145-G-C

44366411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118872599-G-A

44366738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118872273-G-A

http://identifiers.org/hco/5/GRCh38#44366787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118872211-A-C

44366913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118872081-A-G

44367170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118871651-T-G

44367172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118871649-A-G

44367388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118871442-A-G

44367403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118871427-C-T

44367808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118871039-A-T

44367850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118871001-T-A

44367850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118871001-T-C

44367864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118870987-A-G

44367864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118870987-A-T

44367865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118870986-T-A

44367876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118870975-A-T

44367884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118870967-G-T

44367914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118870932-C-T

44368176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118869996-T-C

44368230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118869946-A-G

44368377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118869782-G-A

44368529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118869658-G-A

44368992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118869504-T-A

44369000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118869496-T-A

44369000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118869496-T-C

44369061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118869427-A-G

44369141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118869315-A-G

44369142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118869314-G-A

44369142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118869314-G-C

44369172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118869266-C-G

44369173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118869265-C-G

44369578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118868880-C-G

44369584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118868874-T-C

44369644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118868814-T-C

44369737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118868645-T-C

44370851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118867662-T-C

44370990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118867531-T-A

44371611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118867085-A-T

44371843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118866949-T-C

44371848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118866944-G-A

44371919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118866868-A-G

44372153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118866677-G-A

44372153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118866677-G-C

44372153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118866677-G-T

44372189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118866641-G-A

44372415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118866432-A-G

44372550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118866243-T-C

44372682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118865951-G-A

44372707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118865926-T-A

http://identifiers.org/hco/5/GRCh38#44372771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118865864-A-C

44373032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118865592-T-C

44373033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118865591-T-C

44373036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118865586-G-C

44373183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118865455-A-G

http://identifiers.org/hco/5/GRCh38#44373896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118864753-C-A

44374041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118864619-C-G

44374041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118864619-C-T

44374047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118864613-C-T

44374113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118864541-A-G

44374225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118864421-G-T

44374284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118864373-G-C

44374647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118863824-C-G

44374737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118863734-A-G

44374975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118863496-G-T

44375022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118863450-T-A

44375041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118863430-G-A

44375099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118863371-T-C

44375197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118863272-A-T

44375232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118863237-T-G

44375917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118863083-T-C

44375970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118863024-T-C

44376049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118862898-C-T

44376059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118862887-A-T

44376169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118862787-C-T

44376237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118862712-A-T

44376290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118862659-T-G

44376392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118862557-C-T

44376405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118862545-T-C

44376464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118862486-T-C

44376464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118862486-T-G

http://identifiers.org/hco/5/GRCh38#44376524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118862456-A-C

44376549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118862431-G-A

44376594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118862395-C-T

44376612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118862379-T-A

44376612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118862379-T-C

http://identifiers.org/hco/5/GRCh38#44376731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118862311-C-A

44376744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118862298-A-G

44377072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118861702-T-C

44377261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118861520-G-A

http://identifiers.org/hco/5/GRCh38#44377536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118861290-A-C

44378957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118860974-G-A

44378957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118860974-G-T

44378967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118860961-T-C

44378978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118860951-C-G

http://identifiers.org/hco/5/GRCh38#44378992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118860937-C-A

http://identifiers.org/hco/5/GRCh38#44379536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118860607-C-A

44379847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118860295-G-A

44379885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118860262-T-A

http://identifiers.org/hco/5/GRCh38#44379903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118860247-A-C

44380211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118859976-T-C

44380211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118859976-T-G

44380863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118859501-C-T

44381091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118859357-G-C

44381297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118859192-C-T

44381800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118858725-G-A

44381910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118858641-G-A

44381960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118858587-T-C

44382384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118858156-T-C

44382384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118858156-T-G

44382410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118858130-G-A

44382633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118857908-T-C

44382999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118857537-C-T

44383452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118857111-G-C

44383681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118856889-G-A

44384226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118856315-T-G

44384355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118856182-T-C

http://identifiers.org/hco/5/GRCh38#44384361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118856176-A-C

http://identifiers.org/hco/5/GRCh38#44384688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118855879-C-A

44384792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118855782-C-T

44384797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118855777-T-C

44384826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118855754-C-T

44385240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118855348-A-G

44385402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118855168-G-T

44385714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118854848-A-G

44385725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118854836-T-C

44386077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118854466-G-A

44386077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118854466-G-C

http://identifiers.org/hco/5/GRCh38#44386153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118854391-C-A

44386748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118853835-G-A

44387291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118853296-T-C

44387291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118853296-T-G

http://identifiers.org/hco/5/GRCh38#44387435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118853149-A-C

44387435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118853149-A-T

http://identifiers.org/hco/5/GRCh38#44388247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#118852366-A-C

44388247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: intron variant
orthologous variants: 118852366-A-G

44388747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 118851853-C-T

44388751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 118851849-G-T

http://identifiers.org/hco/5/GRCh38#44388757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#118851843-C-A

44388765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 118851835-G-A

44388765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 118851835-G-C

44388781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 118851819-C-T

44388786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 118851814-G-A

44388786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 118851814-G-T

44388873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 118851727-T-C

http://identifiers.org/hco/5/GRCh38#44388874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#118851726-C-A

44388874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 118851726-C-G

http://identifiers.org/hco/5/GRCh38#44388886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#118851714-C-A

44388937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 118851663-G-A

44388937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 118851663-G-C

44388970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 118851642-G-C

44388970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 118851642-G-T

44389230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 118851385-G-A

44389230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 118851385-G-T

44389279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 118851342-T-C

44389338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 118851280-G-T

44389347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 118851271-T-C

http://identifiers.org/hco/5/GRCh38#44389569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#118851048-C-A

44389569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 118851048-C-T

http://identifiers.org/hco/5/GRCh38#44389570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#118851047-A-C

44389570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 118851047-A-G

44389570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3666
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 118851047-A-T