138795950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 5 prime UTR variant
orthologous variants: 18086761-G-A

138795950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 5 prime UTR variant
orthologous variants: 18086761-G-T

http://identifiers.org/hco/6/GRCh38#138795989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18086720-C-A

138795989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18086720-C-T

138795996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18086713-G-A

138795996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18086713-G-T

138796004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18086705-G-A

138796004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18086705-G-C

138796004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18086705-G-T

138796017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18086690-G-A

138796017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18086690-G-T

http://identifiers.org/hco/6/GRCh38#138796078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18086620-C-A

138796097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18086601-G-A

138796097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18086601-G-T

http://identifiers.org/hco/6/GRCh38#138796168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18086527-C-A

138796168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18086527-C-T

138796186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18086511-C-T

138796301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18086444-A-G

138796427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18086397-G-C

138796446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18086385-T-C

138796550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18086280-A-T

138796560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18086270-C-G

http://identifiers.org/hco/6/GRCh38#138796671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18086184-A-C

138796671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18086184-A-T

138796755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18086097-G-A

138796896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18085952-A-T

138796973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18085869-T-C

138797007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18085848-G-A

138797108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18085433-C-G

138797125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18085416-C-T

138797200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18085335-C-G

138797278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18085269-C-G

138797307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18085242-C-G

138797628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18084578-T-C

138797628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18084578-T-G

138797644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18084562-G-A

http://identifiers.org/hco/6/GRCh38#138797649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18084557-A-C

138797649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18084557-A-T

138802294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18084144-G-C

138802447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18083999-A-G

138802451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18083997-A-G

http://identifiers.org/hco/6/GRCh38#138802457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18083991-A-C

138802474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18083977-A-G

138802478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18083973-C-T

138802497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18083956-C-T

138802518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18083932-T-C

138802545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18083915-A-G

138802565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18083895-C-T

138803321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18083312-C-T

138803455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18083176-A-G

138812912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18078105-T-A

138812912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18078105-T-G

138812946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18078074-T-A

138812958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18078061-T-A

138812958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18078061-T-G

138812983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18078035-A-G

http://identifiers.org/hco/6/GRCh38#138813007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18078011-A-C

http://identifiers.org/hco/6/GRCh38#138813050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18077968-C-A

138813050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18077968-C-T

138813084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18077265-A-T

http://identifiers.org/hco/6/GRCh38#138813099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18077250-A-C

http://identifiers.org/hco/6/GRCh38#138813154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18077188-C-A

138813216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 5 prime UTR variant
orthologous variants: 18077125-G-T

138813267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 5 prime UTR variant
orthologous variants: 18077071-C-T

138813396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18076940-T-C

138813400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18076936-A-G

http://identifiers.org/hco/6/GRCh38#138813428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18076910-A-C

138813428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18076910-A-G

http://identifiers.org/hco/6/GRCh38#138813445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18076864-A-C

138813445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18076864-A-G

138813553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18076631-T-C

138813835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18076416-G-T

138814055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18076199-G-A

http://identifiers.org/hco/6/GRCh38#138814255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18076004-A-C

http://identifiers.org/hco/6/GRCh38#138814289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18075971-C-A

http://identifiers.org/hco/6/GRCh38#138814346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#18075912-C-A

http://identifiers.org/hco/6/GRCh38#138814348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#18075910-C-A

138814348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, undefined
orthologous variants: 18075910-C-G

http://identifiers.org/hco/6/GRCh38#138814350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#18075908-A-C

138814350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, undefined
orthologous variants: 18075908-A-G

138814350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, undefined
orthologous variants: 18075908-A-T

138814357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, undefined
orthologous variants: 18075903-A-G

138814399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18075862-G-A

138814399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18075862-G-C

138814399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18075862-G-T

138814415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, undefined
orthologous variants: 18075846-A-G

138814415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, undefined
orthologous variants: 18075846-A-T

138814459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, undefined
orthologous variants: 18075807-G-A

138814459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, undefined
orthologous variants: 18075807-G-T

138814561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, missense_variant
orthologous variants: 18075710-T-A

138814566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, missense_variant
orthologous variants: 18075705-T-C

138814566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, missense_variant
orthologous variants: 18075705-T-G

138814616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, undefined
orthologous variants: 18075655-T-C

138814637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18075121-T-A

138814718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18075038-T-C

http://identifiers.org/hco/6/GRCh38#138814751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18075007-A-C

138814751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18075007-A-G

138815187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18074637-T-C

138815212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18074618-T-G

138815457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18074360-G-C

138815484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18074332-C-T

http://identifiers.org/hco/6/GRCh38#138816425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18073079-A-C

138816795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18072698-T-C

138816971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18072534-A-G

http://identifiers.org/hco/6/GRCh38#138816973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18072532-C-A

138816973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18072532-C-T

138816996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18072510-C-G

138816996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18072510-C-T

138817127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18072381-T-C

138817732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18071085-A-G

138817905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18070944-G-A

138818000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18070831-C-T

http://identifiers.org/hco/6/GRCh38#138818185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#18070634-A-C

138818291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18070538-A-T

138818374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18070462-C-G

138818374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18070462-C-T

138818397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18070437-A-G

138818397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18070437-A-T

138818576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18070261-G-A

138818777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18070068-A-G

http://identifiers.org/hco/6/GRCh38#138818804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18070042-A-C

138818812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18070036-G-A

138818888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18069933-T-C

138819035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18069798-G-A

138820078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18068444-T-C

138820130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18068405-C-T

138820150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18068386-T-C

138820156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18068379-C-T

138820241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18068303-G-A

138820284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18068244-T-A

138820284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18068244-T-G

138820326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18068201-A-G

138820447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18068091-A-G

138820447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18068091-A-T

http://identifiers.org/hco/6/GRCh38#138820478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18068061-C-A

138820493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18068046-T-C

138820523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18068025-T-C

138820605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18067997-C-T

http://identifiers.org/hco/6/GRCh38#138820654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18067970-A-C

138820697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18067940-G-A

138820818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18067850-T-G

138820853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18067818-A-G

138821028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18067639-G-A

138821113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18067556-A-G

138821264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18067442-G-A

138831764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18060920-T-G

138832137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18060251-G-T

138832229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18060168-A-T

138832242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18060157-C-T

138832385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18060038-G-A

138832397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18060026-C-T

138832414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18060009-C-T

138833431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18058443-G-A

138833956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18058269-C-G

138833969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18058256-C-T

138834406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18057820-T-A

138834406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18057820-T-C

138834540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18057684-G-T

138834892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18056114-T-G

http://identifiers.org/hco/6/GRCh38#138834968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18056092-A-C

138834970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18056090-C-G

138834970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18056090-C-T

138835037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18056028-A-G

http://identifiers.org/hco/6/GRCh38#138835120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18055959-A-C

138835266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18055833-T-C

http://identifiers.org/hco/6/GRCh38#138835721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18055328-A-C

138835721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18055328-A-G

138835798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18055258-C-T

http://identifiers.org/hco/6/GRCh38#138835846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18055198-C-A

138835846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18055198-C-T

138835932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18055113-T-C

138837509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18054937-C-G

http://identifiers.org/hco/6/GRCh38#138837634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18054797-C-A

http://identifiers.org/hco/6/GRCh38#138837651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18054780-A-C

http://identifiers.org/hco/6/GRCh38#138837686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18054713-C-A

http://identifiers.org/hco/6/GRCh38#138837690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18054709-C-A

http://identifiers.org/hco/6/GRCh38#138838239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18051227-A-C

138838239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18051227-A-G

138838239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18051227-A-T

http://identifiers.org/hco/6/GRCh38#138838280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18051186-C-A

138838280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18051186-C-T

http://identifiers.org/hco/6/GRCh38#138838281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18051185-C-A

138838281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18051185-C-T

138838306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18051160-A-G

138838318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18051148-T-A

138838464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18050997-T-G

138838473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18050988-G-A

138838473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18050988-G-T

138838491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18050970-C-T

138838583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18050876-G-A

138838597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18050862-T-C

138838604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18050856-A-G

138838627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18050833-T-A

http://identifiers.org/hco/6/GRCh38#138838640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18050820-C-A

138838640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18050820-C-T

138838655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18050805-G-A

138838655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18050805-G-T

138841842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18050297-A-G

138841875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18050265-T-C

138842001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18050149-G-A

138842002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18050148-T-C

http://identifiers.org/hco/6/GRCh38#138842005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18050145-C-A

138842982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18049887-T-G

138843003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18049866-G-A

138843003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18049866-G-C

138843027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18049842-T-C

138843027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18049842-T-G

138843033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18049836-C-T

http://identifiers.org/hco/6/GRCh38#138843063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18049806-C-A

138843063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18049806-C-T

138843122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: synonymous variant
orthologous variants: 18049747-T-C

138843201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18049668-A-G

138843266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18049599-A-G

http://identifiers.org/hco/6/GRCh38#138843291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18049579-C-A

138843291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18049579-C-T

138843305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18049565-C-G

138843305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18049565-C-T

http://identifiers.org/hco/6/GRCh38#138843312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18049558-C-A

138843312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18049558-C-T

138843366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18049513-G-A

138843381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18049498-G-A

http://identifiers.org/hco/6/GRCh38#138843493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18049386-A-C

138843494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18049385-A-G

138844362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18048635-T-G

138844366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18048631-A-T

http://identifiers.org/hco/6/GRCh38#138844387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18048611-C-A

138844387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18048611-C-T

138844400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18048598-T-G

http://identifiers.org/hco/6/GRCh38#138844487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18048511-C-A

138844487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18048511-C-T

http://identifiers.org/hco/6/GRCh38#138844588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18048410-A-C

138844596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18048402-T-A

138844658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18048342-A-T

138844681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18048319-G-C

http://identifiers.org/hco/6/GRCh38#138844842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18047941-C-A

138844844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18047939-G-A

138844855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18047914-T-C

138844856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18047913-G-T

138844877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18047861-G-A

138844946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18047793-G-A

138846164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18045614-T-A

138846198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18045580-A-G

138846327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18045456-G-A

138846359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18045424-G-A

138846420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18045365-G-T

138846435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18045348-T-A

138846435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18045348-T-C

138846435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18045348-T-G

138846441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18045342-G-A

138846441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18045342-G-T

138846531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 18045259-C-T

138846546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18045244-A-G

138849116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18044327-T-G

http://identifiers.org/hco/6/GRCh38#138849166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18044284-C-A

138849166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18044284-C-G

138849206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18044246-T-C

138849311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18044165-T-C

138849338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18044135-C-T

http://identifiers.org/hco/6/GRCh38#138849388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18044085-C-A

138849388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18044085-C-G

138849388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18044085-C-T

138849401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18044072-G-A

138849401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18044072-G-T

http://identifiers.org/hco/6/GRCh38#138849519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18043952-C-A

138851918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18042087-T-C

138852349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18042004-A-G

138852349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18042004-A-T

138852475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18041879-T-C

138852488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18041866-G-A

138852516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18041837-A-G

138853668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18041719-G-T

138853802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18041602-G-A

138853802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18041602-G-T

138853878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18041506-T-A

138853878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18041506-T-C

138853895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18041489-A-G

138853973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18041410-C-G

138853973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18041410-C-T

138854001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18041382-T-C

138854001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18041382-T-G

138854221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18041167-T-C

138859233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18041129-A-G

138859365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18041022-A-G

138859735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18040720-C-T

138859805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18040651-C-G

138859837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18040628-A-T

138860264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18040304-T-C

138860702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18039891-G-T

138862727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 18039107-T-A

138862811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18039000-G-A

138862811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18039000-G-T

138862831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18038979-T-A

138862831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18038979-T-G

138862837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18038973-T-C

138862854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18038946-G-A

138862854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18038946-G-C

138862854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18038946-G-T

138862929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18038858-T-G

138863044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18038757-A-G

138863053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18038748-A-G

138863140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18038662-G-C

138863202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18038593-A-G

http://identifiers.org/hco/6/GRCh38#138863261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18038534-A-C

138863261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18038534-A-G

138863326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18038470-G-A

138863377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18038426-T-C

138863404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18038399-G-T

http://identifiers.org/hco/6/GRCh38#138863428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18038375-C-A

138863444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18038354-A-G

138864367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18038153-A-G

138864508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18037960-T-C

138864509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18037959-T-C

138864509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18037959-T-G

138864518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18037950-G-A

138864522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18037946-T-C

138864748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18037765-T-C

138864882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18037657-A-G

138864891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18037648-A-G

138864891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18037648-A-T

138865016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18037335-T-C

http://identifiers.org/hco/6/GRCh38#138865017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18037334-C-A

138865017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18037334-C-T

138865021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18037330-A-G

138865052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18037299-T-C

http://identifiers.org/hco/6/GRCh38#138865059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/10/GRCm39#18037292-C-A

138865059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18037292-C-T

138865124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 18037227-C-T

138865254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18037100-T-C

138865290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18037064-A-G

http://identifiers.org/hco/6/GRCh38#138865295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18037059-A-C

138865295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18037059-A-G

138865295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18037059-A-T

138865348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18037030-T-G

138865501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18036890-T-C

138868052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18035637-T-A

138868052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18035637-T-C

138868080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18035620-G-A

http://identifiers.org/hco/6/GRCh38#138868082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18035618-C-A

138868082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18035618-C-T

138868331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18035363-A-G

138868403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18035291-G-A

138868438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18035256-G-A

138868514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18035189-C-T

138868742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18034989-C-G

138869328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18034082-A-G

138869390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18034031-T-A

138869746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18033714-A-G

138870238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18032927-G-A

138870238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18032927-G-T

138870345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18032818-C-T

138870362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18032798-G-C

http://identifiers.org/hco/6/GRCh38#138870418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18032749-C-A

138870512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18032655-C-T

138871306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18032073-C-G

138871421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18031966-G-T

138871443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18031953-T-G

138873406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18031897-T-C

138875142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18023048-T-C

138875196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18023002-T-C

http://identifiers.org/hco/6/GRCh38#138875521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18021500-C-A

138875588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18021439-A-G

http://identifiers.org/hco/6/GRCh38#138876322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18020548-C-A

http://identifiers.org/hco/6/GRCh38#138876357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18020513-C-A

http://identifiers.org/hco/6/GRCh38#138876378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18020492-C-A

138876378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18020492-C-T

138876385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18020485-T-C

138876400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18020470-G-A

138876400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18020470-G-T

138876410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18020450-T-C

138876414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18020446-G-T

http://identifiers.org/hco/6/GRCh38#138876435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18020425-C-A

138876435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18020425-C-T

138876447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18020412-A-T

138876505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18020355-A-G

138876513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: synonymous variant
orthologous variants: 18020347-C-T

138876535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18020325-A-G

138876610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18020064-A-T

138876613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18020061-T-C

http://identifiers.org/hco/6/GRCh38#138876618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18020056-C-A

138876618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18020056-C-T

138876672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18020011-A-G

138876672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18020011-A-T

http://identifiers.org/hco/6/GRCh38#138876689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18019984-A-C

http://identifiers.org/hco/6/GRCh38#138876690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18019983-A-C

138876690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18019983-A-T

138876699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18019974-A-G

138876935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18019298-T-C

138876936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18019297-G-A

138877158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18019146-G-A

138877162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18019142-G-A

138880934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18018874-G-A

138880961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18018849-G-A

138880961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18018849-G-T

138881071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18018739-G-A

138881188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18018623-T-C

138881189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18018622-A-G

138881189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18018622-A-T

138881288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18018515-T-C

http://identifiers.org/hco/6/GRCh38#138882596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18017848-A-C

138882596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18017848-A-G

http://identifiers.org/hco/6/GRCh38#138882810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18017635-A-C

http://identifiers.org/hco/6/GRCh38#138883071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18017386-C-A

138884845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18016660-T-C

138885388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18016455-G-A

138885388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18016455-G-T

http://identifiers.org/hco/6/GRCh38#138885432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18016411-C-A

http://identifiers.org/hco/6/GRCh38#138885521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18016317-C-A

138885521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18016317-C-G

138885521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18016317-C-T

138885533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18016305-A-G

http://identifiers.org/hco/6/GRCh38#138885723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18016113-A-C

138885723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18016113-A-T

138885753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18016083-C-T

138885754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18016082-C-T

138885762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18016074-C-T

138885881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18015960-G-A

138885881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18015960-G-C

http://identifiers.org/hco/6/GRCh38#138885903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18015938-C-A

138885903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18015938-C-T

138885908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18015933-A-T

138885979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18015864-T-C

138885999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18015844-G-A

138886000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18015843-G-A

138886831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18014643-G-T

http://identifiers.org/hco/6/GRCh38#138886958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18014518-C-A

138886958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18014518-C-G

138886958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18014518-C-T

138886978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18014501-T-G

138887026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18014453-A-G

138887026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18014453-A-T

138887081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18014400-T-A

138887104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18014385-G-T

138888042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18013469-G-A

138888167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18013362-T-C

138888793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18012878-T-C

138888840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18012831-T-G

138888866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18012805-G-T

138888871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18012800-A-G

138888876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18012795-G-A

138888876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18012795-G-T

138888976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18012707-G-A

138888976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18012707-G-T

http://identifiers.org/hco/6/GRCh38#138889161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18012521-C-A

138889161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18012521-C-T

138889344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18012359-A-T

http://identifiers.org/hco/6/GRCh38#138889643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18012143-A-C

138889654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18012132-G-A

138889944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18011859-T-C

138890044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18011794-T-A

138890371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18011615-G-A

138890371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18011615-G-C

138890415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18011577-G-C

138890463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18011437-A-T

138890466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18011434-G-T

http://identifiers.org/hco/6/GRCh38#138890485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18011390-C-A

138890485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18011390-C-T

138890523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18011349-T-C

138890523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18011349-T-G

138895244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18009251-G-A

http://identifiers.org/hco/6/GRCh38#138895252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18009243-A-C

138895335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18009193-T-C

138895369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18009159-G-A

http://identifiers.org/hco/6/GRCh38#138896058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18008591-C-A

138896058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18008591-C-T

138896211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18008400-G-A

138896231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18008382-A-T

138897080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18008046-C-T

138897081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18008045-A-G

138897115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18008011-T-C

138897956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18007825-T-C

http://identifiers.org/hco/6/GRCh38#138898230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18007510-A-C

138898379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18007384-C-G

138900178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18007182-C-T

138900193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18007158-A-G

138900893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18006560-G-A

138900893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18006560-G-C

138900977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18006482-T-C

138901111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: missense variant
orthologous variants: 18006348-G-T

138901203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18006268-G-A

138901203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18006268-G-T

138901213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18006261-T-C

138901460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18006066-T-C

138901480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18006045-T-G

138901572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18005846-T-C

138901753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18005672-A-G

138901796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18005629-C-T

138901802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18005627-T-C

138901828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18005601-T-C

138901850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18005580-A-G

138902134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18005411-G-A

138902327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18005233-C-T

http://identifiers.org/hco/6/GRCh38#138902373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18005184-C-A

138902373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: intron variant
orthologous variants: 18005184-C-T

138902738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 3 prime UTR variant
orthologous variants: 18004663-G-T

138902749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 3 prime UTR variant
orthologous variants: 18004645-A-G

138902750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 3 prime UTR variant
orthologous variants: 18004644-G-T

138902818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 3 prime UTR variant
orthologous variants: 18004576-T-C

http://identifiers.org/hco/6/GRCh38#138902903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18004496-A-C

http://identifiers.org/hco/6/GRCh38#138902922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18004482-C-A

138902922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 3 prime UTR variant
orthologous variants: 18004482-C-T

138902926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 3 prime UTR variant
orthologous variants: 18004478-T-C

138903667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 3 prime UTR variant
orthologous variants: 18002318-T-G

138903912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 3 prime UTR variant
orthologous variants: 18002197-G-T

http://identifiers.org/hco/6/GRCh38#138904046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21118
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18002106-A-C