http://identifiers.org/hco/17/GRCh38#67377300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#107361577-C-A

67377300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 107361577-C-G

67377382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 5 prime UTR variant
orthologous variants: 107361493-C-T

67377396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 107361479-G-A

67377437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 107361461-C-T

67377546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 5 prime UTR variant
orthologous variants: 107361359-G-A

67377546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 5 prime UTR variant
orthologous variants: 107361359-G-C

67377546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 5 prime UTR variant
orthologous variants: 107361359-G-T

67377679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 5 prime UTR variant
orthologous variants: 107361225-C-T

67377755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 5 prime UTR variant
orthologous variants: 107361147-T-G

http://identifiers.org/hco/17/GRCh38#67378022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107360877-C-A

67378022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 5 prime UTR variant
orthologous variants: 107360877-C-T

http://identifiers.org/hco/17/GRCh38#67378228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107360694-C-A

67378228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107360694-C-T

67378235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107360687-T-A

67378235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107360687-T-C

67378235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107360687-T-G

http://identifiers.org/hco/17/GRCh38#67378268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107360660-C-A

67378268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107360660-C-T

67378301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, undefined
orthologous variants: 107360626-G-A

67378301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, undefined
orthologous variants: 107360626-G-T

67378364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, undefined
orthologous variants: 107360572-C-T

67378516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107360419-C-T

67378708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, undefined
orthologous variants: 107360239-G-C

http://identifiers.org/hco/17/GRCh38#67378917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#107360025-C-A

http://identifiers.org/hco/17/GRCh38#67379006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107359905-C-A

67379006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107359905-C-G

67379006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107359905-C-T

67379010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107359901-G-A

67379057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107359854-C-G

http://identifiers.org/hco/17/GRCh38#67379145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107359770-A-C

67379341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107359588-T-C

67379415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107359481-G-A

67379415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107359481-G-T

http://identifiers.org/hco/17/GRCh38#67379435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107359461-A-C

http://identifiers.org/hco/17/GRCh38#67379436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107359460-A-C

67379436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107359460-A-G

67379511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107359365-G-T

67379971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107358836-T-C

67380004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107358821-G-A

67380004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107358821-G-T

67380044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107358775-C-G

67380302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107358561-T-G

67380352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107358504-G-A

67380352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107358504-G-C

67382035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107357604-C-T

67382198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107357436-C-T

67384152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107355323-T-C

67384291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107355196-C-T

http://identifiers.org/hco/17/GRCh38#67384407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107355076-C-A

67384407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107355076-C-T

67384467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107354930-C-G

67384581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107354826-G-A

67384582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107354825-C-T

67384636-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107354736-A-T

67384832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107354606-G-T

67384839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107354599-A-G

67386419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107353709-C-G

67386419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107353709-C-T

67386434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107353689-C-T

67386705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107353387-G-T

67386787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107353291-A-G

67386889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107353184-C-T

67390115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107349906-C-T

67390137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107349884-G-A

67390220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107349798-T-C

67390455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107349634-T-C

67390723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107349450-A-G

67391328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107348530-G-A

67391362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107348472-C-T

67391405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107347484-T-C

67391467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107347428-T-G

67391607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107347289-A-G

67393742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107343573-T-A

67393762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107343553-T-A

67395356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107342456-C-T

67395379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107342433-C-G

67395442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107342366-C-T

67396009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107341190-A-G

67396009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107341190-A-T

67396034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107341165-C-T

67396303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107340902-C-T

67397440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107340403-A-T

67397674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107340161-G-A

67400183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107338107-T-C

67400246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107338058-C-G

67400573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107337630-T-C

67400768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107337420-A-G

67400770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107337418-C-G

67400770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107337418-C-T

67401078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107337055-G-T

67401082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107337051-G-A

http://identifiers.org/hco/17/GRCh38#67403272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107333931-C-A

67403287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107333917-T-G

67403439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107333760-A-G

67403483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107333713-A-G

67403495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107333701-G-A

67403529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107333677-T-C

http://identifiers.org/hco/17/GRCh38#67403583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107333618-C-A

67404184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107331858-C-T

67404233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107331813-A-G

67404310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107331751-C-T

67404466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107331604-A-G

http://identifiers.org/hco/17/GRCh38#67409976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107327954-C-A

67409976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107327954-C-G

67409993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107327924-G-C

67411156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107327014-T-C

67411234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107326951-A-T

67417687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107323302-C-T

67418480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107322801-T-C

http://identifiers.org/hco/17/GRCh38#67419130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107321455-A-C

67419215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107321390-C-T

67419544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107321097-G-C

67420935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107320096-A-G

67421202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107319824-T-C

67421278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107319765-T-C

67421960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, undefined
orthologous variants: 107319123-A-G

67422175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, undefined
orthologous variants: 107318914-G-T

67422261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, undefined
orthologous variants: 107318835-C-G

67423913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107316947-G-A

67426048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107316358-T-C

67427857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107315031-C-T

http://identifiers.org/hco/17/GRCh38#67427860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107315028-C-A

67431400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107313599-T-C

67432750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107312582-C-G

67432750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107312582-C-T

67439405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107309437-G-T

67439431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107309412-A-G

67439577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107309284-C-G

http://identifiers.org/hco/17/GRCh38#67441094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107308302-C-A

67441483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 107307987-C-T

67441691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107307784-G-C

67441815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107307668-A-G

http://identifiers.org/hco/17/GRCh38#67442061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107307421-C-A

67442061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107307421-C-T

67442895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107306204-T-C

67443005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107306108-T-C

67443098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107306027-C-T

67443142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107305993-C-T

67443148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107305987-G-C

67443370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107305813-T-C

67443452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107305731-T-C

67445795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, undefined
orthologous variants: 107304336-G-A

67445911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107304221-A-G

67448608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107303167-C-T

67448670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107303100-C-T

67448750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107303035-T-C

67448790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107303015-G-C

67448898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107302906-C-G

67448913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107302891-C-T

67449402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107302324-T-G

67449482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107302226-C-T

67449668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107302030-C-T

67449710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107301991-G-A

67449710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107301991-G-T

67450105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107300791-C-T

67453203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, undefined
orthologous variants: 107298057-T-C

67453349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107297897-G-C

67453393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, undefined
orthologous variants: 107297854-C-G

67453628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107297636-G-A

67453694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107297420-A-T

67453824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107297293-A-G

67453828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107297289-G-C

http://identifiers.org/hco/17/GRCh38#67453886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107297229-A-C

67453893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107297221-T-C

67453902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107297214-T-A

http://identifiers.org/hco/17/GRCh38#67454268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107296876-A-C

67454269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107296875-A-T

http://identifiers.org/hco/17/GRCh38#67454270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107296874-C-A

67454521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107296400-T-C

67454570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107296376-T-G

http://identifiers.org/hco/17/GRCh38#67454712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107296237-C-A

67454858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107296093-C-T

67455156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107295895-A-G

67455256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107295801-T-C

67460000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107290816-T-G

67460001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107290815-C-T

67460016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107290808-G-C

http://identifiers.org/hco/17/GRCh38#67460162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107290665-A-C

67460197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107290633-C-G

67460210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107290621-G-A

67461343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107290370-C-T

67461374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107290343-G-A

67464214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107289438-A-G

67464489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107289144-G-A

http://identifiers.org/hco/17/GRCh38#67464574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107289065-A-C

http://identifiers.org/hco/17/GRCh38#67464671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107288973-C-A

67464671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107288973-C-G

67466679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107288584-A-G

67466732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107288532-A-G

67466768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107288497-G-C

67467849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107287506-C-T

67467899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107287454-T-C

67467925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107287427-C-T

67473638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107286476-C-T

67473667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107286430-C-G

67473701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107286405-T-C

67473701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107286405-T-G

67473744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107286360-A-G

67473767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107286300-G-A

67473910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107286166-T-C

67473942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107286148-C-T

67474136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107285964-T-G

67474149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107285951-C-T

67474552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107285609-G-A

67474564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107285597-T-G

67474580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107285526-G-C

67474581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107285525-G-A

67475922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107284396-G-A

67476064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107284278-A-G

67476112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107284239-C-G

67477841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107282876-C-T

67477899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107282838-G-A

67477905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107282832-G-C

67477970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107282766-G-A

67478333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107281907-G-A

67478984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107281345-G-A

67479173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107281200-G-A

67479183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107281190-C-T

http://identifiers.org/hco/17/GRCh38#67479295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107281033-C-A

67479295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107281033-C-T

67479331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107280996-C-T

67479410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107280919-C-T

67479509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107280815-G-A

67479655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107280104-T-G

67479709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107280044-A-T

67479800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107279955-G-A

67479869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107279884-C-T

67480184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107279581-G-A

67480260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107279505-G-A

67480527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107278416-A-G

67480533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107278410-T-C

67480608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107278331-G-A

67480643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107278291-T-C

67480707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107278231-A-G

67481214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107278007-T-C

67481279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107277935-A-G

67481428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107277817-A-G

67482120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107277299-T-G

67482134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107277285-C-T

67482135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107277284-G-A

67482242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107277191-T-C

67482769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107275799-G-C

67482811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107275761-A-G

67482937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107275669-C-T

67483001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107275611-C-T

67483002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107275610-G-A

67483040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107275577-G-T

67483141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107275457-G-A

67483533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107275178-G-A

67483542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107275169-T-C

67483651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107275050-G-A

http://identifiers.org/hco/17/GRCh38#67483914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107274892-C-A

67483914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107274892-C-T

67484268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107274080-A-G

http://identifiers.org/hco/17/GRCh38#67484573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107273786-A-C

67484573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107273786-A-T

67485151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107273347-A-G

http://identifiers.org/hco/17/GRCh38#67485226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107273259-A-C

67485226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107273259-A-G

http://identifiers.org/hco/17/GRCh38#67485413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107273136-C-A

67485413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107273136-C-T

67485666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107273090-C-T

67485677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107273079-C-T

67485933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107272872-C-T

67485947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107272854-C-T

67486022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107272780-T-C

67486024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107272778-G-T

67486514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107272312-G-C

67486690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107271874-G-A

67487560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107271230-T-C

67487565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107271225-G-A

67487992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107270797-A-T

67488007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107270782-T-G

67488021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107270772-T-A

http://identifiers.org/hco/17/GRCh38#67488023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107270770-A-C

67488039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107270754-G-C

67488304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, undefined
orthologous variants: 107270484-G-A

67490267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107268128-T-A

67490267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107268128-T-G

67490407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107268032-A-T

67490450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107267990-C-T

67490517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107267933-G-A

67490966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107267548-T-C

67491227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107267307-A-G

67491414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107267148-A-G

67491499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107267062-A-G

67491504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107267057-G-A

http://identifiers.org/hco/17/GRCh38#67492135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107266628-C-A

67493325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107263785-T-A

67493325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107263785-T-G

67493558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107263556-C-T

67493759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107263342-G-T

http://identifiers.org/hco/17/GRCh38#67493785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107263315-A-C

67493860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107263240-A-G

67493869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107263231-C-T

67493995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107263129-C-T

67494050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107263083-G-A

67494581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107262778-T-C

67494624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107262741-T-C

67495989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107260881-C-T

67496044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107260834-A-G

67496230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107260645-T-A

67496247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107260628-C-T

67502059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107257831-G-C

67502104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107257792-G-A

67502105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107257791-T-C

67502314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107257580-C-T

67502444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107257463-A-G

67502474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107257433-G-A

67502474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107257433-G-C

67507155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107252439-A-G

67515003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107247443-G-T

http://identifiers.org/hco/17/GRCh38#67515849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107246471-A-C

67516009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107246310-T-C

67516123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107246192-C-T

67516351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107245992-A-G

67516364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107245979-C-G

67516656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107245711-A-G

67517527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107244710-G-T

67517553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107244685-T-C

67517672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107244569-A-G

67517768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107244482-A-T

67517849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107244283-C-T

67517944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107244096-A-G

67518167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107243688-A-T

67518177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107243635-G-C

67518193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107243617-G-C

http://identifiers.org/hco/17/GRCh38#67518226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107243582-C-A

67519848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107241167-C-T

67519975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107241082-T-A

67520230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107240851-G-A

67520533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107240565-T-G

67520655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107240281-C-T

67520818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107240035-G-C

67520978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107239898-C-T

67520979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107239897-G-A

67520979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107239897-G-T

67521495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107239205-C-T

67521563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107239120-A-T

67521576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107239078-G-T

67521632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107239016-G-A

67521632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107239016-G-C

67522096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107238799-G-A

67522158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107238734-G-A

67522228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107238673-C-T

67522454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107238425-T-C

67523325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107236987-G-A

67523328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107236984-G-C

67523381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107236932-T-C

67523518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107236789-C-T

67523535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107236768-G-T

67523684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107236608-G-A

67523712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107236579-C-T

67523791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107236501-G-T

67525253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107235788-C-T

67525388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107235646-A-G

67525802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107235267-A-G

67525825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107235246-T-G

67525845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107235226-C-T

67525958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107234917-C-T

67526341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107234664-A-G

http://identifiers.org/hco/17/GRCh38#67528893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107232641-C-A

67528893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107232641-C-T

67528943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, undefined
orthologous variants: 107232588-C-T

67528993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, undefined
orthologous variants: 107232539-G-A

67529081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, undefined
orthologous variants: 107232447-G-A

http://identifiers.org/hco/17/GRCh38#67529155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107232373-C-A

67529241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107232283-G-A

67529408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107232115-G-C

http://identifiers.org/hco/17/GRCh38#67530484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107230720-A-C

67531259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107230356-G-T

67531332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107230293-C-G

67531332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107230293-C-T

67531485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107230173-C-T

67531534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107230123-C-T

67531536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107230121-C-G

67531720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107229936-C-T

67531836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107229845-C-T

67532009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107229484-G-A

67532465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107228727-T-C

67532703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107228498-G-A

67532703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107228498-G-T

67532743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107228449-G-A

67532743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107228449-G-C

67532761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107228429-G-A

67532761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107228429-G-T

67532787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron variant
orthologous variants: 107228403-G-T

http://identifiers.org/hco/17/GRCh38#67532856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107228330-C-A

67532856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: missense variant
orthologous variants: 107228330-C-G

67532856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: missense variant
orthologous variants: 107228330-C-T

67532997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107228201-G-A

67532997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107228201-G-T

67533045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107228186-T-C

http://identifiers.org/hco/17/GRCh38#67533080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107228154-C-A

67533080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107228154-C-T

67533672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107227939-C-T

67533765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107227857-G-A

67533827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107227808-G-A

67533827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107227808-G-T

67534749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107227129-A-G

67534881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107226931-C-T

67535087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107226739-A-T

67535150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107226676-T-C

67535432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107226434-C-T

http://identifiers.org/hco/17/GRCh38#67535442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107226424-C-A

67542317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107220908-A-G

67542384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107220832-A-T

67543203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107219785-G-A

67543203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107219785-G-T

67544198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107218852-C-G

67544710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107218465-C-T

67548681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107216788-T-G

67549518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107214958-C-T

67549710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107214784-T-A

67549722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107214772-T-C

67549849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107214567-C-T

67549917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107214380-G-C

67549954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107214342-G-A

67549956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107214340-T-A

67549956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107214340-T-C

67550073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107214234-G-A

http://identifiers.org/hco/17/GRCh38#67550246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107214071-C-A

67550301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107214018-G-A

67550460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107213823-G-A

http://identifiers.org/hco/17/GRCh38#67552165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107212620-C-A

67552181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107212609-T-C

67552258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 107212498-A-G

http://identifiers.org/hco/17/GRCh38#67552397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107212363-C-A

67552399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107212361-T-C

67553040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107212232-C-G

67553263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107211961-T-C

67553309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107211915-T-G

http://identifiers.org/hco/17/GRCh38#67553357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107211865-C-A

67553357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107211865-C-T

http://identifiers.org/hco/17/GRCh38#67553382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107211840-C-A

67553455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107211781-A-G

67553477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107211754-G-C

67553477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107211754-G-T

67553516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107211715-T-A

67553516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107211715-T-C

67553577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107211657-T-A

67553577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107211657-T-C

67553585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107211649-T-A

67553585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107211649-T-C

67553587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107211647-T-A

67553587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107211647-T-C

67553596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107211638-A-G

67553596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107211638-A-T

67553671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107211565-T-A

67553671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107211565-T-C

67553675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107211561-A-G

67553675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107211561-A-T

67553807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107211418-G-T

67556265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107208410-G-T

67557070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107207086-A-G

67557133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107207003-G-C

67557674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107206477-G-T

67557738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107206437-A-G

67557794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107206386-C-T

67558327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107205882-T-C

67558996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107205016-A-G

67559232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107204941-A-G

67559386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107204809-A-G

67559410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107204786-G-A

67559483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107204718-G-A

67559483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107204718-G-C

67559483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107204718-G-T

67560163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107203654-G-A

67560344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107203502-T-C

67560684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107202773-C-T

67561932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107201765-A-G

67561947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107201749-C-G

67562167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107201551-C-G

67562208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107201510-G-A

67562593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107201148-T-C

67562665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107201079-C-G

67562769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107201023-C-T

67562782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107201010-G-A

67563203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107200019-A-G

67563230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107199986-C-T

67563314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107199912-C-T

67563693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107199565-T-C

67563737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107199519-G-T

67563792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107199464-G-A

67568047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107198557-C-T

67568065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107198539-G-A

67568163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107198370-C-T

67568371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107198197-A-G

67568373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107198195-G-A

67569137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107197345-T-A

67569142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107197340-A-G

67569353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107197129-A-G

67569737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107196746-G-A

67570312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107196449-G-T

67570424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107196400-A-G

67570493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107196321-T-C

67570557-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107196253-A-T

67570611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107196195-G-A

67570618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107196188-C-T

67570758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107196068-T-G

67570797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107196034-A-T

67570821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107196010-G-T

67570824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107196007-G-T

67570830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107196001-G-T

67570906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107195940-A-G

67570995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107195869-A-G

67571002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107195862-T-C

67571011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107195853-G-T

67571942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107195235-A-G

http://identifiers.org/hco/17/GRCh38#67572023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107195158-C-A

67572079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107195113-G-A

67572084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107195108-C-T

67572356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107194860-T-C

67572742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107194600-G-A

67572748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107194594-T-A

67572748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107194594-T-G

67572771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107194584-C-T

67573089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107193360-G-A

67573173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107193276-C-T

67573488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107192987-T-A

67574189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107192343-T-C

67575008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107190552-C-T

67575074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107190442-T-G

67575238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107190005-C-T

67575437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107189783-A-G

http://identifiers.org/hco/17/GRCh38#67576240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107189365-C-A

67576240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107189365-C-T

67576371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107189206-C-G

67576513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107189102-T-C

67576517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107189098-G-A

67576726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107188891-G-C

67576764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107188853-G-A

67577921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107187333-T-C

67577937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107187320-T-A

67578013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107187251-G-T

67578083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107187190-C-T

67578111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107187162-G-A

67578111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107187162-G-T

67578153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107187127-T-A

67578153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107187127-T-C

67578153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107187127-T-G

67578169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107187111-T-C

67578255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 107187025-A-G

http://identifiers.org/hco/17/GRCh38#67578287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107186983-C-A

67578287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107186983-C-G

67578287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107186983-C-T

67578293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107186977-G-A

67578293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107186977-G-C

67578293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107186977-G-T

http://identifiers.org/hco/17/GRCh38#67578384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107186929-C-A

67578384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107186929-C-G

67578384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107186929-C-T

http://identifiers.org/hco/17/GRCh38#67578407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#107186927-C-A

http://identifiers.org/hco/17/GRCh38#67579422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107185454-A-C

67579450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107185426-C-T

67579451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107185425-A-G

67579609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107185281-T-A

67580062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107185049-G-A

67582152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107183714-C-T

67582190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107183680-T-C

67582271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107183609-G-A

67582319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107183580-A-T

67582399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107183508-C-T

67582453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107183454-A-G

67582457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107183450-G-A

67582484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107183423-G-A

67583009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107182919-G-A

67587883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107179752-T-C

67588812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107179520-C-T

67588856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107179480-C-T

67589014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107179105-A-G

67589214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107178932-C-T

http://identifiers.org/hco/17/GRCh38#67593751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107177136-C-A

67593802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107177081-C-G

67594165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107176704-G-A

http://identifiers.org/hco/17/GRCh38#67594256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107176614-A-C

67594384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107176499-T-C

67594709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107176213-C-G

67594709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107176213-C-T

67594736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107176184-C-G

67594836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107176084-T-C

67594836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107176084-T-G

67594845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107176079-T-C

67594941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107175982-A-G

67594941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107175982-A-T

67595016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107175899-T-C

67595149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107175762-T-C

67595891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107174155-T-C

67595892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107174154-A-G

67596336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107173532-G-C

67596455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107172586-C-T

67600871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107169554-A-G

67601089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107169338-G-A

http://identifiers.org/hco/17/GRCh38#67601177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107169253-C-A

67601287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107169150-T-G

67601408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107168953-G-C

67601437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107168917-C-T

http://identifiers.org/hco/17/GRCh38#67602036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107168185-A-C

67602115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107168108-C-T

67602446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107167808-T-G

http://identifiers.org/hco/17/GRCh38#67603067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#107167034-A-C

67603068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107167033-G-T

67603072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107167029-G-C

67604004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107166652-T-C

67605125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107165526-G-T

67605232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107165418-A-G

67605370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107165281-T-C

67605441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107165208-C-T

67605725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107164927-T-C

67605754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107164899-C-T

67605892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107164791-G-T

67605911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107164760-A-G

67606489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107163551-G-A

67606702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107163353-C-T

http://identifiers.org/hco/17/GRCh38#67606937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107163121-C-A

67607043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107163024-G-A

67609888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107160044-C-T

http://identifiers.org/hco/17/GRCh38#67609951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107159983-C-A

67610006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107159938-C-G

67610026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107159919-A-G

67611196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107159010-A-G

67611266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107158965-G-A

67611266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107158965-G-T

67611803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107158434-A-G

67611902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107158353-T-C

67611920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107158335-C-G

67611920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107158335-C-T

67611962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107158284-C-G

67611962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107158284-C-T

67611963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107158283-T-C

67611975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107158271-C-T

67612004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107158252-C-T

67612205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107158110-A-G

http://identifiers.org/hco/17/GRCh38#67612220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107158096-C-A

67612254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107158061-G-T

http://identifiers.org/hco/17/GRCh38#67612261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107158054-C-A

67612261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107158054-C-T

67612264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107158051-G-T

67612280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107158035-G-A

67612280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107158035-G-T

67612287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107158028-G-A

67612287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107158028-G-T

67612305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107158010-A-G

67612354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157961-A-G

67612369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157944-G-A

67612369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157944-G-T

67612404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157914-T-C

http://identifiers.org/hco/17/GRCh38#67612406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107157912-C-A

67612406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157912-C-G

67612406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157912-C-T

67612426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157894-T-C

67612510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157835-A-G

http://identifiers.org/hco/17/GRCh38#67612519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107157826-A-C

http://identifiers.org/hco/17/GRCh38#67612568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107157777-C-A

67612598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157747-G-A

http://identifiers.org/hco/17/GRCh38#67612613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107157732-C-A

67612613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157732-C-T

67612687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157657-A-G

67612713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157631-G-C

67612725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157619-G-C

67612741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157603-G-A

67612741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157603-G-T

http://identifiers.org/hco/17/GRCh38#67612745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107157599-A-C

67612745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157599-A-G

67612838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157490-A-G

67612838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157490-A-T

http://identifiers.org/hco/17/GRCh38#67613276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107157352-C-A

67613276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157352-C-G

67613276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157352-C-T

67613281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157347-A-G

67613331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157298-G-A

67613373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107157242-G-T

67615239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107156323-C-T

67615597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107155892-A-G

67615950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107155524-C-T

67616032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107155419-T-G

67616091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107155353-T-G

http://identifiers.org/hco/17/GRCh38#67616703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107154999-C-A

67616716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107154986-G-C

67616878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107154854-C-T

http://identifiers.org/hco/17/GRCh38#67619752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107151793-A-C

67619752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107151793-A-G

http://identifiers.org/hco/17/GRCh38#67619770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107151775-A-C

http://identifiers.org/hco/17/GRCh38#67619862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107151694-A-C

67619874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107151682-G-A

http://identifiers.org/hco/17/GRCh38#67619919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107151671-C-A

67620424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107150778-A-G

http://identifiers.org/hco/17/GRCh38#67620838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107150431-A-C

67620889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107150380-G-A

67622997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107148697-G-A

67623156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107148596-T-A

http://identifiers.org/hco/17/GRCh38#67623189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107148563-C-A

67623213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107148539-G-A

67623827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107148030-T-C

67624051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107147788-G-C

67624051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107147788-G-T

67624074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107147765-A-G

67627683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107147044-G-A

67627683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107147044-G-T

http://identifiers.org/hco/17/GRCh38#67627825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107146931-A-C

67628350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107146743-A-G

67628350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107146743-A-T

67628392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107146703-A-T

67628704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107146330-G-A

67628704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107146330-G-T

67628705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107146329-G-A

67628942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107146094-T-G

67628952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107146073-T-C

67629010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107146019-C-T

67630185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107144525-T-C

67631684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107143368-T-G

67631685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107143367-T-A

67631694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107143366-A-T

67631998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107143093-T-C

67632009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107143082-G-A

67632009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107143082-G-T

67632019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107143072-A-T

http://identifiers.org/hco/17/GRCh38#67632044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107143053-C-A

67632044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107143053-C-T

http://identifiers.org/hco/17/GRCh38#67632084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107143015-C-A

http://identifiers.org/hco/17/GRCh38#67632101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107142998-C-A

67632120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107142964-G-A

http://identifiers.org/hco/17/GRCh38#67632134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107142950-C-A

67632134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107142950-C-T

67632313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107142767-T-C

http://identifiers.org/hco/17/GRCh38#67632332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107142755-C-A

67632332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107142755-C-G

67632355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107142736-G-A

67632355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107142736-G-C

http://identifiers.org/hco/17/GRCh38#67632412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107142678-A-C

67632412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107142678-A-G

67632766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107142316-C-T

67632945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107142070-T-G

67633213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107141819-A-G

http://identifiers.org/hco/17/GRCh38#67637069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107141121-A-C

67637085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107141106-C-G

67637090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107141101-C-T

67637136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107141041-G-T

67637137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107141040-C-T

67637138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107141039-T-C

67637287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107140894-C-T

67637425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107140737-C-T

67637427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107140735-G-A

67637472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107140683-G-T

67637475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107140680-C-T

67637503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107140656-C-T

67637650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107140528-C-G

67637650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107140528-C-T

67637739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107140447-T-G

http://identifiers.org/hco/17/GRCh38#67637782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107140399-C-A

67637789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107140392-T-C

67637791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107140390-A-G

67637830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107140151-G-A

67637830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107140151-G-T

67637854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107140127-G-T

67637865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107140118-T-G

67637943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107139894-A-G

http://identifiers.org/hco/17/GRCh38#67637966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#107139872-C-A

http://identifiers.org/hco/17/GRCh38#67638002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#107139837-C-A

67638002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107139837-C-T

67638029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107139810-G-A

67638029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107139810-G-T

67638030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107139809-G-A

http://identifiers.org/hco/17/GRCh38#67638076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#107139763-C-A

http://identifiers.org/hco/17/GRCh38#67638150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#107139689-C-A

67638150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107139689-C-T

http://identifiers.org/hco/17/GRCh38#67638153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#107139686-C-A

67638153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107139686-C-T

http://identifiers.org/hco/17/GRCh38#67638180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#107139679-A-C

67638189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107139670-A-G

http://identifiers.org/hco/17/GRCh38#67638209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#107139652-C-A

67638209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107139652-C-T

http://identifiers.org/hco/17/GRCh38#67638231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#107139631-C-A

67638256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107139605-G-A

67638256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107139605-G-T

http://identifiers.org/hco/17/GRCh38#67638391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#107139511-C-A

67638408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107139495-A-G

67638437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107139472-T-C

67638465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107139444-C-T

67638480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107139441-C-T

http://identifiers.org/hco/17/GRCh38#67638486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107139435-C-A

67638486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107139435-C-T

67638550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107139369-C-T

67638575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107139344-A-G

67639570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107138336-G-T

http://identifiers.org/hco/17/GRCh38#67640058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107137843-A-C

67640058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107137843-A-T

67640089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107137806-T-C

67640098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107137797-C-T

67640250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107137659-G-A

67643634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107135791-T-C

67643976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107135054-G-A

67644135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107134895-C-T

67650990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107133723-C-T

67651087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107133628-G-A

67651115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107133600-G-T

67652486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107131975-C-T

67652628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107131834-C-T

67654452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107130078-T-G

67655152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107129718-G-A

67656429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107128572-G-C

67656547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107128456-G-A

67656547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107128456-G-C

67657260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107127534-G-T

67657464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107127310-T-C

http://identifiers.org/hco/17/GRCh38#67657598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107127218-C-A

http://identifiers.org/hco/17/GRCh38#67669367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107125418-C-A

67669396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107125390-G-A

67669396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107125390-G-C

67669396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107125390-G-T

67669397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107125389-T-C

67669397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107125389-T-G

http://identifiers.org/hco/17/GRCh38#67669407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107125379-C-A

67669407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107125379-C-T

http://identifiers.org/hco/17/GRCh38#67669411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107125375-C-A

67669411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107125375-C-T

67669474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107125359-A-G

67669474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107125359-A-T

67669491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107125342-G-T

http://identifiers.org/hco/17/GRCh38#67669742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107125092-A-C

67670118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107125041-T-C

67670237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107124919-C-T

67670392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107124744-C-G

67671294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107124535-T-C

67672901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107121255-C-G

67673308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107120846-T-C

67673744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107120416-T-G

67675456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107117141-A-G

67675521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107117076-G-A

67675580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107117017-T-C

http://identifiers.org/hco/17/GRCh38#67675614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107116979-C-A

67675614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107116979-C-T

67676735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107116142-G-A

67676918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107115991-T-C

67676975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107115946-C-G

67677010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107115919-C-T

67678332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107115109-T-A

67678530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107114910-G-A

67678778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107114652-T-A

67678784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107114646-T-C

67678793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107114644-G-T

67678805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107114632-T-C

67678817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107114620-A-G

67679000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107114452-C-T

67679169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107114341-A-G

67679379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107114196-C-T

67679681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107113886-T-C

67679850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107113719-G-A

67680358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107113201-G-C

67680366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107113193-A-G

67680391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107113175-G-A

67683292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107110140-T-A

67683506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107109947-C-T

67684690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107109716-C-G

http://identifiers.org/hco/17/GRCh38#67684787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107109604-A-C

67685246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107109201-G-C

67685766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107108680-T-C

67686356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107108300-A-T

http://identifiers.org/hco/17/GRCh38#67687236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107107450-A-C

67687394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107107286-G-C

67687394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107107286-G-T

67687712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107106998-C-G

67687712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107106998-C-T

67688028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107106663-A-T

67688317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107106372-A-G

67688337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107106352-T-A

67688337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107106352-T-C

67688348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107106341-A-T

67688484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107106194-T-C

67689598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107104968-T-C

67690025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107104530-A-G

67690133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107104416-G-T

67692440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107103595-T-C

http://identifiers.org/hco/17/GRCh38#67692523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107103527-C-A

67692523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107103527-C-G

67692523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107103527-C-T

67692553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107103501-T-C

67692553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107103501-T-G

http://identifiers.org/hco/17/GRCh38#67692554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107103500-C-A

67692554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107103500-C-T

67692715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107103339-C-T

http://identifiers.org/hco/17/GRCh38#67692772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107103282-C-A

67692772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107103282-C-T

67692784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107103270-T-C

67692890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107103164-T-A

67692890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107103164-T-C

67692899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107103155-A-G

67692957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107103091-T-A

67692957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107103091-T-G

67692960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107103088-T-C

67693084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107102964-G-A

67693109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107102711-G-T

67693137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107102685-G-A

67693137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107102685-G-T

67693580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107102214-G-A

67693726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107102075-G-A

67693726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107102075-G-T

67693754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107102047-A-G

67693828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107101986-G-T

http://identifiers.org/hco/17/GRCh38#67693887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107101936-C-A

67693928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107101894-A-G

67693968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107101854-A-G

67693973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107101849-G-T

67694109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107101627-G-T

http://identifiers.org/hco/17/GRCh38#67694159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107101586-A-C

67694289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107101511-A-G

67694295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107101505-A-G

http://identifiers.org/hco/17/GRCh38#67694351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107101447-C-A

http://identifiers.org/hco/17/GRCh38#67694551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107101243-C-A

67694602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107101206-T-C

67694753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107101073-G-T

67695082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107100745-A-G

67695189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107100641-G-C

67695234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107100607-T-C

67695236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107100605-G-A

http://identifiers.org/hco/17/GRCh38#67695272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107100562-C-A

67695709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107100137-A-G

67695834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107100013-T-A

http://identifiers.org/hco/17/GRCh38#67696446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107099509-C-A

67696550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107099406-C-T

67696663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107099290-T-C

http://identifiers.org/hco/17/GRCh38#67696734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107099212-C-A

http://identifiers.org/hco/17/GRCh38#67696735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#107099211-A-C

67696773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107099173-G-A

67697021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107098947-G-T

67697034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107098934-T-C

67697034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107098934-T-G

67697064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107098904-C-T

67697140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107098836-T-C

67697221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107098751-T-C