18904323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139347650-C-T

18904564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139347440-T-C

http://identifiers.org/hco/1/GRCh38#18904642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139347362-C-A

18905069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139347021-T-C

18905077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139347017-G-T

18905210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139346938-G-T

18905211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139346937-T-C

18905211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139346937-T-G

18905213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139346935-A-G

18905222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139346926-G-A

18905372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139346795-G-T

http://identifiers.org/hco/1/GRCh38#18905500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139346673-C-A

18905500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139346673-C-T

18905565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139346607-C-T

18905680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139346515-G-A

18905784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139346417-T-C

http://identifiers.org/hco/1/GRCh38#18905821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139346377-C-A

18905821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139346377-C-T

18905968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139346232-G-A

http://identifiers.org/hco/1/GRCh38#18906011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139346175-C-A

18906011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139346175-C-T

18906041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139346144-A-G

http://identifiers.org/hco/1/GRCh38#18906158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139346033-A-C

18906158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139346033-A-G

18906164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139346027-A-G

18906171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139346020-G-A

18906171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139346020-G-T

18906173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139346018-G-A

http://identifiers.org/hco/1/GRCh38#18906203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139345988-C-A

18906204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139345987-T-C

18906213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139345982-G-A

18906213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139345982-G-T

http://identifiers.org/hco/1/GRCh38#18906319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139345912-C-A

18906319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139345912-C-T

http://identifiers.org/hco/1/GRCh38#18906360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139345859-C-A

18906360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139345859-C-G

18906399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139345823-A-G

18906445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139345777-G-A

18906445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139345777-G-T

18906486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139345747-G-A

18906486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139345747-G-T

18906964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139345280-G-A

18906967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139345277-G-A

18906967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139345277-G-T

18907286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 139344957-G-A

18907286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 139344957-G-T

18907391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139344870-T-C

18907421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139344838-T-C

http://identifiers.org/hco/1/GRCh38#18907422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139344837-C-A

18907484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139344766-G-T

http://identifiers.org/hco/1/GRCh38#18907503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139344747-C-A

18907503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139344747-C-T

18907560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139344692-G-C

18907560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139344692-G-T

18907564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139344688-G-A

18907564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139344688-G-T

18907640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 139344610-A-G

http://identifiers.org/hco/1/GRCh38#18907678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#139344572-C-A

18907678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 139344572-C-T

18907703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 139344553-A-G

http://identifiers.org/hco/1/GRCh38#18907752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139344487-C-A

18907799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139344450-G-A

18907799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139344450-G-T

18907914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139344321-T-C

18907953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139344280-T-A

18907953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139344280-T-C

18908042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139344195-C-T

http://identifiers.org/hco/1/GRCh38#18908139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139344115-C-A

18908139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139344115-C-G

18908139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139344115-C-T

18908179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139344080-G-A

18908287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139343969-A-G

http://identifiers.org/hco/1/GRCh38#18908417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139343866-C-A

18908417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139343866-C-G

18908417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139343866-C-T

http://identifiers.org/hco/1/GRCh38#18908440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139343843-A-C

18908440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 3 prime UTR variant
orthologous variants: 139343843-A-G

http://identifiers.org/hco/1/GRCh38#18908592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139343711-C-A

18908592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: missense variant
orthologous variants: 139343711-C-T

18908693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139343615-T-A

18908759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139343546-G-T

18910251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139342472-G-T

http://identifiers.org/hco/1/GRCh38#18910259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139342460-C-A

18910259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139342460-C-T

18910281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139342439-G-T

18910304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139342412-A-G

18910320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139342396-C-G

18910488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139342224-G-A

18910488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139342224-G-C

18910535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139342171-A-G

18910550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139342157-A-G

18910550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139342157-A-T

18910564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139342143-G-T

18910602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139342132-A-G

18910687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139342053-G-A

18910734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139342008-C-T

18910996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139341778-C-T

18911031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139341746-T-C

18911036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139341741-G-A

http://identifiers.org/hco/1/GRCh38#18911237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139341556-C-A

18911237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139341556-C-T

http://identifiers.org/hco/1/GRCh38#18911264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139341532-C-A

18911264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139341532-C-T

18911336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139341473-G-A

18911336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139341473-G-C

18911336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139341473-G-T

18911385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 139341426-T-C

18911876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139341288-A-G

18911886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139341279-G-A

18911886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139341279-G-T

http://identifiers.org/hco/1/GRCh38#18913559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139338892-C-A

18913559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139338892-C-G

18913875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139338723-G-A

18913875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139338723-G-T

18914270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139338468-T-C

18914270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139338468-T-G

18914294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139338444-C-T

18914535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139338186-G-A

18914689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139337996-G-A

18914689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139337996-G-C

18916887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139335069-C-T

18916893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139335063-G-A

18916933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: missense variant
orthologous variants: 139335023-G-A

18916933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: missense variant
orthologous variants: 139335023-G-C

18916933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: missense variant
orthologous variants: 139335023-G-T

18916948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: missense variant
orthologous variants: 139335008-C-T

18917006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: missense variant
orthologous variants: 139334950-C-G

18917006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: missense variant
orthologous variants: 139334950-C-T

18917075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139334882-G-C

18917098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139334860-T-C

18917101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139334857-G-A

18917101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139334857-G-T

18917109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139334849-T-C

18917109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139334849-T-G

18917538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139334443-T-C

18918045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139334145-A-G

18918106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139334082-G-A

18918211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139334014-G-T

18918262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139333974-G-A

18918278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139333958-A-G

18918290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139333944-G-A

18918290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139333944-G-T

18918408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, missense_variant
orthologous variants: 139333825-T-A

18918408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, missense_variant
orthologous variants: 139333825-T-G

http://identifiers.org/hco/1/GRCh38#18918413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139333820-C-A

18918538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139333696-G-A

18918614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139333581-T-A

18918614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139333581-T-C

http://identifiers.org/hco/1/GRCh38#18918616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139333541-C-A

18918616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139333541-C-T

18918635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139333522-G-C

18918635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139333522-G-T

18918649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139333508-A-G

18918649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139333508-A-T

18918850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139333220-G-A

http://identifiers.org/hco/1/GRCh38#18918859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139333211-C-A

18918859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139333211-C-G

18918879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139333172-A-G

18919246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139332784-C-T

18919250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139332780-G-T

18919470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139332589-C-G

18919508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139332557-A-G

18919508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139332557-A-T

18919587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139332492-G-A

18919587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139332492-G-T

http://identifiers.org/hco/1/GRCh38#18919602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139332479-C-A

18919845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139332255-G-A

18919845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139332255-G-T

18919883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139332215-G-A

18919883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139332215-G-T

18920054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139332084-A-G

18920057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139332081-A-G

18920063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139332075-A-G

18920075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139332061-C-T

18920167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139331963-C-T

18920169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139331961-G-A

http://identifiers.org/hco/1/GRCh38#18921245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139330416-C-A

18921245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139330416-C-T

18921268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139330397-G-A

18921777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139330041-T-C

18921889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139329947-T-C

18922067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139329767-A-G

18922161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, undefined
orthologous variants: 139329694-G-C

18922161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, undefined
orthologous variants: 139329694-G-T

http://identifiers.org/hco/1/GRCh38#18922874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139329170-C-A

18922976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139329094-G-A

18923022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139329049-C-T

http://identifiers.org/hco/1/GRCh38#18923113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139328980-C-A

18923232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139328876-C-T

http://identifiers.org/hco/1/GRCh38#18923685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139328398-C-A

18923689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139328394-A-G

18923951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139328184-A-G

18923992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139328143-G-A

18924134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139327984-G-A

18924160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139327958-G-A

18926094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139326997-A-T

18926195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139326922-T-A

18926213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139326907-C-T

18926352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139326790-G-C

18926369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, undefined
orthologous variants: 139326773-G-C

http://identifiers.org/hco/1/GRCh38#18926618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#139326543-C-A

18926664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, undefined
orthologous variants: 139326497-G-T

18926866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, undefined
orthologous variants: 139326294-G-A

http://identifiers.org/hco/1/GRCh38#18926930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#139326237-C-A

18926963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139326207-A-G

18926964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139326206-G-T

18927019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, undefined
orthologous variants: 139325691-C-T

18927167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139325552-G-A

18927167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139325552-G-T

18927297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139325412-C-G

18927490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139325219-A-G

18927935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, undefined
orthologous variants: 139324952-C-T

18927944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139324943-G-A

18927969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139324918-G-A

18928093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139324796-C-T

18928182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, undefined
orthologous variants: 139324696-G-A

18928190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, undefined
orthologous variants: 139324687-C-T

18928406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139324502-C-T

18928616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139324320-G-A

18928673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139324273-G-A

18929856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139323455-T-C

18929919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139323393-A-G

18929967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139323346-A-G

18930117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139323218-A-G

18930233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139323116-T-C

18930465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139322919-G-A

http://identifiers.org/hco/1/GRCh38#18931250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139322375-C-A

18931627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139322090-T-G

18931888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139321842-G-A

18931888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139321842-G-T

18932125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139321570-C-T

18936778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139320444-G-A

18936856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139320394-A-G

http://identifiers.org/hco/1/GRCh38#18936974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139320265-C-A

18937353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139319929-A-G

http://identifiers.org/hco/1/GRCh38#18937617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139319652-C-A

18937617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139319652-C-T

18938025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139318620-T-C

http://identifiers.org/hco/1/GRCh38#18938053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139318594-C-A

18938117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139318533-G-A

18938154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139318496-C-T

18938362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139318374-T-C

18938554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139318223-G-A

18938738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139318075-C-T

18938793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139318022-G-T

http://identifiers.org/hco/1/GRCh38#18939053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139317802-C-A

18939094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139317765-G-A

http://identifiers.org/hco/1/GRCh38#18939353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139317605-C-A

18939353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139317605-C-T

18939593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139317408-G-C

18939654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139317354-G-C

18939738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139317299-T-A

18939820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139317216-C-T

18940239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139316914-C-G

18940239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139316914-C-T

18940315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139316855-T-C

18940611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139316518-A-G

18940615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139316514-G-A

18940619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139316510-G-A

18940623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139316506-A-G

18940627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139316502-G-A

18940836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139315846-G-A

18940979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139315717-G-A

18940979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139315717-G-T

18941137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139315553-C-T

18941420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139315333-C-G

18941420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139315333-C-T

18941696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139315108-G-A

18942486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139314711-A-G

18942699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139314501-C-T

18943434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139314288-C-T

18943646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139314154-A-G

18943675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139314125-G-A

18943956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139313868-T-C

18944012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139313815-G-A

18944679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139312868-C-T

18944796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139312755-T-G

http://identifiers.org/hco/1/GRCh38#18944837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139312713-C-A

18944850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139312700-G-A

18944855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139312695-G-C

18944900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139312650-A-T

18945264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139312327-T-C

18945269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139312322-G-A

18945269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139312322-G-C

18945644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139311954-A-G

18945733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139311901-C-T

18945739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139311895-C-T

18946003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139311678-G-A

18946222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139311478-A-T

18946883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139311178-G-A

18947167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139310996-G-A

18947750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139310578-T-G

18947881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139310452-G-A

18947884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139310449-C-T

18947992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139310365-G-A

http://identifiers.org/hco/1/GRCh38#18947997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139310360-C-A

18947997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139310360-C-T

http://identifiers.org/hco/1/GRCh38#18948292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139310152-C-A

18948403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139310045-C-G

18948403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139310045-C-T

18948591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139309844-G-T

18948614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139309819-T-C

18948616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139309817-G-A

18948652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139309771-G-C

18948661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139309757-C-G

18949322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, undefined
orthologous variants: 139308979-G-A

18949771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, undefined
orthologous variants: 139308557-G-A

18949829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, undefined
orthologous variants: 139308512-G-A

18949829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, undefined
orthologous variants: 139308512-G-C

18949829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, undefined
orthologous variants: 139308512-G-T

18949956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139308379-T-G

18950117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139308223-G-C

18950184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139308159-C-T

18950480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139307905-G-T

18950668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139307736-A-T

18950760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139307658-G-A

http://identifiers.org/hco/1/GRCh38#18950933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139307488-C-A

18950933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139307488-C-T

18951449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139307038-C-G

18951449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139307038-C-T

18952577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139306232-A-T

18952746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, undefined
orthologous variants: 139306083-G-A

18952746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, undefined
orthologous variants: 139306083-G-C

18952752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron_variant, undefined
orthologous variants: 139306077-G-C

18952830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139306001-G-A

18952830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139306001-G-C

18952937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139305919-G-A

18953060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139305813-G-C

18953793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139304549-C-T

18954448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139303957-C-T

18954687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139303779-C-T

http://identifiers.org/hco/1/GRCh38#18954728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139303738-C-A

18955015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139303463-C-G

18955053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139303425-A-G

18955076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139303407-G-T

18955142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: intron variant
orthologous variants: 139303337-G-T

http://identifiers.org/hco/1/GRCh38#18955812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139302762-C-A

18955812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: missense variant
orthologous variants: 139302762-C-T

http://identifiers.org/hco/1/GRCh38#18956058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139302522-C-A

18956058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: missense variant
orthologous variants: 139302522-C-T

18956178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: missense variant
orthologous variants: 139302402-G-A

18956178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: missense variant
orthologous variants: 139302402-G-T

http://identifiers.org/hco/1/GRCh38#18956235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139302345-C-A

18956235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: missense variant
orthologous variants: 139302345-C-G

18956235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: missense variant
orthologous variants: 139302345-C-T

18956243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: synonymous variant
orthologous variants: 139302337-G-A

18956243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: synonymous variant
orthologous variants: 139302337-G-C

18956243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: synonymous variant
orthologous variants: 139302337-G-T

18956370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 5 prime UTR variant
orthologous variants: 139302219-T-A

18956370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 5 prime UTR variant
orthologous variants: 139302219-T-C

18956444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 5 prime UTR variant
orthologous variants: 139302145-C-T

18956572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 5 prime UTR variant
orthologous variants: 139302074-G-A

18956598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 5 prime UTR variant
orthologous variants: 139302048-C-T

18956647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 5 prime UTR variant
orthologous variants: 139301999-G-A

18956647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27006
most severe consequence: 5 prime UTR variant
orthologous variants: 139301999-G-T