http://identifiers.org/hco/4/GRCh38#105894837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132656553-A-C

105894867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 132656507-G-A

http://identifiers.org/hco/4/GRCh38#105895023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132656357-C-A

105895023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132656357-C-T

105895030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132656350-C-T

105895174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132656230-C-T

105895301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132656111-G-A

105895301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132656111-G-C

105895301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132656111-G-T

http://identifiers.org/hco/4/GRCh38#105895417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132655992-A-C

http://identifiers.org/hco/4/GRCh38#105895491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132655921-C-A

105895491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 132655921-C-T

105895497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 132655915-G-A

105895497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 132655915-G-T

105895565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 132655850-T-C

105895580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 132655843-T-C

http://identifiers.org/hco/4/GRCh38#105895589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#132655834-C-A

105895589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 132655834-C-G

105895589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 132655834-C-T

105895593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 132655830-C-T

105895868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 132655685-G-A

http://identifiers.org/hco/4/GRCh38#105895878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#132655675-C-A

105895878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 132655675-C-G

105895957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 132655624-G-A

105895957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 132655624-G-T

105895994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132655618-A-T

105896051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, undefined
orthologous variants: 132655605-G-A

105896051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, undefined
orthologous variants: 132655605-G-T

105896834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132654941-T-C

105896993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132654798-C-T

http://identifiers.org/hco/4/GRCh38#105897273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132654512-C-A

105897691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132654122-G-A

105897848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132653960-T-C

105898023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132653784-T-C

105898060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132653726-A-G

105898151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132653654-C-T

105898222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132653582-T-C

105898411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132653286-G-A

105898433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132653264-C-G

105898433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132653264-C-T

105898490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132653243-T-C

105898542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132653191-G-T

http://identifiers.org/hco/4/GRCh38#105898557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132653170-C-A

105898751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132652552-A-G

105898841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132652451-T-C

105898873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132652419-C-G

105899813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132650653-C-T

http://identifiers.org/hco/4/GRCh38#105900056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132650417-A-C

105900072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132650399-A-G

105900073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132650398-T-A

105900086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132650385-A-G

105900510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132650024-C-T

105900569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132649972-C-T

http://identifiers.org/hco/4/GRCh38#105900824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132649717-A-C

105900824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132649717-A-T

105900837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132649710-T-G

105900874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132649673-T-A

105900913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132649634-C-T

105901063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132649484-A-G

105901095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132649443-T-G

105901530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132648785-A-G

105901624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132648718-G-A

105901624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132648718-G-C

105901636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132648706-T-C

105901644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132648698-C-T

105901794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132648545-A-T

105902101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132648250-T-G

105902102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132648249-G-C

105902510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132646799-T-G

105902721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132646551-G-T

105903279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132645975-G-A

http://identifiers.org/hco/4/GRCh38#105903393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132645880-A-C

105903395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132645878-A-G

105904111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132645312-A-G

105904373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132645114-C-T

105904611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132644863-G-A

105904611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132644863-G-C

105905104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132644753-A-G

105905238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132644650-A-G

105905242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132644646-A-T

105905447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132644415-C-T

105905567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132644311-T-C

105905568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132644310-C-T

105905723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132644161-T-C

105905930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132643970-T-A

105905944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132643956-C-T

105906914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132643636-A-G

105907081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132643484-A-G

http://identifiers.org/hco/4/GRCh38#105907285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132643282-C-A

105907291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132643276-A-G

105907300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132643267-C-G

105907318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132643192-T-G

105907386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132643113-C-T

105907414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132643099-A-T

105907490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132643032-C-T

105907687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132642883-G-A

105907802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132642764-T-G

105907911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132642669-G-A

105908022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132642566-A-G

105908067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132642530-T-C

105908099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132642499-T-C

105908210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132642397-C-T

105908358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132642268-C-T

http://identifiers.org/hco/4/GRCh38#105908432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132642171-A-C

105908448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132642155-T-C

105908486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132642117-T-A

105910227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132639930-T-A

http://identifiers.org/hco/4/GRCh38#105910257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132639900-C-A

105910496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132639677-A-G

105910548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132639624-A-G

http://identifiers.org/hco/4/GRCh38#105910812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132639424-C-A

105911210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132639007-T-A

105911242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132638555-A-G

105911325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132638472-T-A

105911381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132638419-A-G

105911815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132637976-C-G

105911815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132637976-C-T

105912373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132637202-T-C

105912490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132637075-T-A

105912535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 132637030-T-C

105912542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 132637023-G-A

105912542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 132637023-G-T

105912614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132636945-G-A

105912614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132636945-G-C

105912614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132636945-G-T

105912635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132636924-T-C

105912800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132636786-G-C

105913162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132636286-C-T

105913443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132635986-T-C

105913849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132635674-A-G

105913900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132635626-G-C

105914593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132635113-A-G

105914766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132634958-A-G

105914787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132634937-G-C

105914966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132634773-G-T

105915382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132634265-G-C

105915382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132634265-G-T

105915550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132634143-C-T

105915729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132633969-T-G

105915880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132633822-A-G

105916026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132633684-G-A

105916039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132633671-A-G

105916218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132633473-G-A

105916336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132633292-C-T

http://identifiers.org/hco/4/GRCh38#105916424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132633221-A-C

105916424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132633221-A-T

105916878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132632739-T-C

105916883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132632734-G-A

105917228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132632459-G-C

105917283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132632401-G-A

105917299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132632392-A-G

105917320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132632371-C-T

105917409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132632293-T-G

105917410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132632292-T-C

http://identifiers.org/hco/4/GRCh38#105917893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132631903-A-C

105918072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132631747-C-T

105918205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132631615-G-A

105918235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132631585-C-T

http://identifiers.org/hco/4/GRCh38#105918354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132631466-A-C

105918763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132631088-G-A

105918788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132631063-C-T

105918836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132631026-C-T

105920061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132630372-G-A

105920075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132630358-T-G

105920089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132630344-A-G

105920101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132630332-T-C

http://identifiers.org/hco/4/GRCh38#105920107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132630326-C-A

105920107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132630326-C-G

105920155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132630278-C-T

105920376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132630102-A-G

http://identifiers.org/hco/4/GRCh38#105920412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132630066-A-C

105920548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132629940-A-G

105920558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132629930-T-C

105920558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132629930-T-G

105920560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132629928-C-G

105920572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132629915-T-C

105920705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132629600-T-C

105920727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132629578-G-T

105920834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132629482-T-G

105921152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132629194-A-T

105921378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132629011-T-G

105921489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132628914-G-A

105921771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132628640-T-C

105921826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132628585-C-T

105922033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132628406-A-G

105922033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132628406-A-T

105922239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132628241-T-A

105922422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132628088-C-T

105922782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132627932-G-A

105922931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132627812-G-A

105922985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132627757-G-A

http://identifiers.org/hco/4/GRCh38#105922996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132627746-A-C

http://identifiers.org/hco/4/GRCh38#105923021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132627721-A-C

105923471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132627282-C-G

105923477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132627276-T-C

105923615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132627166-T-C

http://identifiers.org/hco/4/GRCh38#105924041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132626722-C-A

105924041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132626722-C-G

105924041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132626722-C-T

http://identifiers.org/hco/4/GRCh38#105924155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132626595-C-A

105924160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132626590-T-C

105924196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132626551-G-A

105924367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132626439-T-C

105924772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132626077-T-C

105924822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132626033-G-C

105924850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132626005-T-C

105925027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132625830-A-G

105925610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132625219-T-C

105925714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132625120-T-C

105925808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132625026-T-G

105925861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132624988-T-A

http://identifiers.org/hco/4/GRCh38#105925980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132624881-C-A

105925995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132624864-T-C

105926071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132624792-G-A

105926071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132624792-G-T

105926076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132624787-C-G

105926076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132624787-C-T

105926179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132624686-T-A

105926251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132624615-T-C

105926258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132624608-C-G

105926258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132624608-C-T

105926477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132624154-C-T

105926498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132624133-C-T

105926604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132624052-A-G

http://identifiers.org/hco/4/GRCh38#105926788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132623897-A-C

105926788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132623897-A-G

105926790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132623895-A-G

105927028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132623572-G-A

105927028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132623572-G-C

105927028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132623572-G-T

105927039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132623569-T-G

105927075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132623551-T-C

105927075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132623551-T-G

105927113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132623519-A-T

105927114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132623518-T-C

105927114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132623518-T-G

http://identifiers.org/hco/4/GRCh38#105927133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132623499-A-C

105927133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132623499-A-G

105927133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132623499-A-T

http://identifiers.org/hco/4/GRCh38#105927142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132623490-C-A

105927142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132623490-C-G

105927142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132623490-C-T

http://identifiers.org/hco/4/GRCh38#105927149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132623484-A-C

105927149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132623484-A-G

105927149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132623484-A-T

105927162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132623470-G-A

105927162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132623470-G-T

105927173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132623460-T-G

105927196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132623445-A-G

105927229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132623413-A-G

105927369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132623279-G-A

http://identifiers.org/hco/4/GRCh38#105927416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132623232-A-C

http://identifiers.org/hco/4/GRCh38#105927533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132623123-A-C

105927533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132623123-A-G

105927533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132623123-A-T

105927539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132623117-G-A

105927539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132623117-G-C

105927539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132623117-G-T

105927549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132623116-T-A

105927596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132623072-T-C

105928026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132622690-C-G

105928026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132622690-C-T

105928310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132622393-T-C

105928310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132622393-T-G

105930254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132622131-C-T

105930291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132622100-A-G

105930453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132621997-G-T

http://identifiers.org/hco/4/GRCh38#105930533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132621924-C-A

105930802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132621703-T-C

105930821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132621685-G-A

105930846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132621661-C-T

http://identifiers.org/hco/4/GRCh38#105931283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132621193-C-A

105931319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132621162-A-G

105931355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132621124-G-A

105931410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132621068-A-G

105931907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132620900-G-A

105931918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132620891-C-T

http://identifiers.org/hco/4/GRCh38#105931953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132620850-C-A

105931983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132620821-T-C

105932118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132620680-T-G

105932191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132620609-G-A

105932219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132620585-C-G

105932230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132620574-T-G

http://identifiers.org/hco/4/GRCh38#105932631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132620204-C-A

105932652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 132620183-C-T

105932710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 132620125-G-A

105932710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 132620125-G-T

105932825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132620018-T-C

105933083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132619752-G-C

105933150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132619684-G-A

http://identifiers.org/hco/4/GRCh38#105933211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132619624-A-C

105933284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132619542-A-G

105933429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132619406-T-G

105933575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132619270-C-T

105933892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132618913-T-C

105933946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132618866-T-G

http://identifiers.org/hco/4/GRCh38#105934504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132618437-C-A

105934713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132618249-T-C

105934770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132618182-T-A

105934777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132618118-A-G

105934990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132617672-A-G

105935038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132617623-A-G

105935092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132617569-C-T

105935142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132617520-C-T

105935481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132617222-C-T

105935485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132617218-C-T

105935723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132616980-C-T

105935727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132616977-T-A

105935950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132616756-T-C

105936626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132616159-C-T

105936838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615939-G-A

http://identifiers.org/hco/4/GRCh38#105936858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132615923-C-A

105936861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615920-G-A

105936861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615920-G-T

105936866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615915-G-T

105936877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615903-T-A

105936880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615900-T-A

105936880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615900-T-C

105936947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615835-A-G

105936948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615834-G-A

105936948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615834-G-C

105936949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615833-A-G

http://identifiers.org/hco/4/GRCh38#105936965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132615817-C-A

105936975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615809-G-A

http://identifiers.org/hco/4/GRCh38#105936977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132615807-A-C

105936977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615807-A-G

105937001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 132615782-G-A

105937035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132615748-C-T

105937153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615630-T-C

105937240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615542-G-T

http://identifiers.org/hco/4/GRCh38#105937413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132615378-C-A

105937413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615378-C-T

105937757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614799-T-A

105937802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614761-T-C

105938150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614361-T-C

105938150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614361-T-G

105938163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614348-G-T

http://identifiers.org/hco/4/GRCh38#105938181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132614332-C-A

105938181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614332-C-T

105938198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614321-T-C

105938216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614302-T-C

http://identifiers.org/hco/4/GRCh38#105938223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132614295-C-A

105938223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614295-C-T

105938267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614256-A-G

105938339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132614183-T-C

105938495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614038-A-G

http://identifiers.org/hco/4/GRCh38#105938509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132614027-C-A

105938509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614027-C-T

http://identifiers.org/hco/4/GRCh38#105938533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132614004-C-A

105938533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614004-C-T

105938550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132613987-T-C

http://identifiers.org/hco/4/GRCh38#105939162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132613385-A-C

105939283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132613247-T-C

105939571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132613014-A-G

105939930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132612701-G-A

105939930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132612701-G-T

105939934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132612697-G-A

http://identifiers.org/hco/4/GRCh38#105939969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132612668-C-A

http://identifiers.org/hco/4/GRCh38#105939984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132612662-C-A

105939984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132612662-C-T

http://identifiers.org/hco/4/GRCh38#105940018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132612636-C-A

105940018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132612636-C-G

105940018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132612636-C-T

105940053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132612610-T-C

105940248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132612416-T-C

105940281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132612384-G-T

105940335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132612337-A-T

105940386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132612292-G-C

105940386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132612292-G-T

105940406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132612274-T-C

http://identifiers.org/hco/4/GRCh38#105940699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132612046-A-C

105940699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132612046-A-G

105940709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132612036-A-G

http://identifiers.org/hco/4/GRCh38#105940727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132612014-A-C

105940727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132612014-A-G

105940743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132611999-T-C

http://identifiers.org/hco/4/GRCh38#105940957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132611779-C-A

105941435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132611625-G-A

105941724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132611305-A-G

105941899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132611153-G-A

105942276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132610848-A-G

105942570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: missense variant
orthologous variants: 132610549-C-T

http://identifiers.org/hco/4/GRCh38#105942603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132610516-C-A

105942603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: synonymous variant
orthologous variants: 132610516-C-T

105942669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: missense variant
orthologous variants: 132610450-A-T

http://identifiers.org/hco/4/GRCh38#105942723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132610182-C-A

105942734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132610172-T-C

105942736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132610170-G-T

105942758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132610149-A-G

http://identifiers.org/hco/4/GRCh38#105942808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132610101-A-C

105942808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132610101-A-G

105942823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132610089-T-C

http://identifiers.org/hco/4/GRCh38#105942849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132610061-C-A

105942849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132610061-C-T

105942862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132610048-C-G

105943194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132609817-G-C

105943260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132609759-G-A

105943313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132609710-A-G

105943732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132609248-T-C

105943770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132609212-A-G

http://identifiers.org/hco/4/GRCh38#105944292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132608524-C-A

105944698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132608139-G-A

105944790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132608067-G-C

105944827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132608028-T-C

105948301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132606786-A-T

http://identifiers.org/hco/4/GRCh38#105948337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132606750-C-A

105948542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132606622-A-G

105948982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132606225-C-T

105949033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132606176-T-G

105949165-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132606061-T-A

105949330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132605891-A-T

105949548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132605706-G-A

http://identifiers.org/hco/4/GRCh38#105949685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132605571-C-A

105949694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132605562-T-A

105949859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132605402-T-A

105949950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132605309-T-C

105949983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132605276-C-T

105950013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132605246-A-G

http://identifiers.org/hco/4/GRCh38#105950049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132605211-C-A

105950200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132605029-T-C

105950320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132604908-T-C

105950926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132604861-C-T

105951388-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132604409-A-T

105951428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132604338-T-G

105951660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132604150-C-T

105951934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132603904-G-A

105952046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132603793-T-G

105952200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132603658-T-C

105953265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132603030-A-G

105953267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132603028-A-G

105953289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132603010-T-G

105953535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132602787-T-C

105953573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132602762-A-G

105954157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132602214-T-C

105954161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132602210-G-C

105954189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132602179-C-T

105954237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132602129-C-T

105954543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132601523-G-A

105954809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132601287-G-C

105954907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132601158-A-G

105954985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132601083-G-A

105955019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132601050-G-A

105955027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132601042-G-A

105955089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132600993-T-C

105955380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132600769-A-G

105955460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132600697-A-G

105955485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132600672-T-G

105955504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132600653-C-T

105955643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132600520-C-T

105955652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132600511-G-A

105955824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132600368-T-A

105955824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132600368-T-C

105955930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132600267-A-G

105956012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132600207-T-A

105956015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132600204-A-G

http://identifiers.org/hco/4/GRCh38#105956032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132600189-A-C

105956032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132600189-A-T

105956153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132600119-T-C

105956250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132600060-T-A

105956385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132599955-A-G

105956404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132599938-A-G

105956425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132599918-C-G

105956535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132599825-T-C

105956834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132599568-T-A

105957181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132599182-G-A

105957183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132599180-A-G

105957223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132599114-A-T

105957398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132598962-C-T

105957931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132598419-T-C

105958005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132598345-A-G

105958127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132598200-C-T

105958128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132598199-G-A

105958293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132597404-T-C

105958315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132597382-C-T

http://identifiers.org/hco/4/GRCh38#105958393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132597334-C-A

105958393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132597334-C-G

http://identifiers.org/hco/4/GRCh38#105958436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132597292-C-A

105958436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132597292-C-T

http://identifiers.org/hco/4/GRCh38#105958447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132597279-A-C

105958561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132597156-A-G

105958574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132597136-T-A

105958574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132597136-T-C

105958633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132597038-A-G

105958633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132597038-A-T

105958861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132596797-G-A

105958861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132596797-G-T

105958946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596699-T-C

105958961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596684-C-G

105959245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132596472-G-A

105959245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132596472-G-T

105959393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132596335-T-G

105959429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132596299-T-C

105959475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132596252-G-A

105959497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132596233-A-T

105959550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132596186-T-G

105959572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132596165-A-G

105960364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132595677-G-A

105960377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132595664-G-A

105960948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132595136-A-G

105961330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132594856-G-C

105961444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132594749-G-A

http://identifiers.org/hco/4/GRCh38#105961492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132594666-C-A

105961513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132594645-G-A

105961577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132594585-C-G

105961816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132594342-C-T

105961904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132594263-C-T

105962104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132594092-G-A

105962278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132593924-A-G

105962301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132593897-G-A

105962311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132593889-C-T

105965435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132593275-A-T

105965614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132593079-T-C

105965665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132593040-C-T

http://identifiers.org/hco/4/GRCh38#105965856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132592810-C-A

105965884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132592780-A-T

105966059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132592618-G-A

105966162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132592517-A-G

105966216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132592474-C-T

http://identifiers.org/hco/4/GRCh38#105966252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#132592436-A-C

105966252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132592436-A-G

105966254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132592434-G-A

105966544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132592198-T-C

105966743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132592159-G-A

105966820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132592093-G-A

105966820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132592093-G-T

105966870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132592048-G-A

105966953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132591971-G-A

105966953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132591971-G-T

105967037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132591906-G-A

105967037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132591906-G-T

105967062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132591881-T-C

http://identifiers.org/hco/4/GRCh38#105967087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132591856-A-C

105967087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132591856-A-G

105967219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132591740-A-T

105967636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132591355-T-C

105967704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132591293-T-A

105967753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132591250-A-G

105967753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132591250-A-T

105967839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132591164-A-T

105968203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132590808-C-T

105968593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132590578-T-C

105968692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132590482-T-C

105968740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132590427-G-C

105968761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132590406-A-G

http://identifiers.org/hco/4/GRCh38#105968777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132590391-C-A

105968777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132590391-C-G

105968777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132590391-C-T

105968878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132590289-G-A

105968878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132590289-G-C

105968878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132590289-G-T

105968967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 132590200-G-A

105969020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132590151-G-T

105969108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132590077-A-G

http://identifiers.org/hco/4/GRCh38#105969127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132590058-C-A

105969127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132590058-C-T

105969204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132589983-A-T

http://identifiers.org/hco/4/GRCh38#105969208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132589979-C-A

105969208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132589979-C-G

105969208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132589979-C-T

105969236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132589953-T-A

105969242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132589947-G-C

105969273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132589916-A-T

http://identifiers.org/hco/4/GRCh38#105969342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132589860-C-A

105969342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132589860-C-T

105969396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132589813-T-C

http://identifiers.org/hco/4/GRCh38#105969398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132589811-C-A

105969407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132589802-G-T

105969441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132589760-G-T

http://identifiers.org/hco/4/GRCh38#105969460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132589741-C-A

105969513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132589702-T-C

105970031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132589213-G-T

105970046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132589198-G-A

105970046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132589198-G-T

105970059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132589187-A-G

105970144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132589133-A-G

105970176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132589102-A-T

105970180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132589095-A-G

105970180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132589095-A-T

105970182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132589093-G-C

105970184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132589091-G-A

http://identifiers.org/hco/4/GRCh38#105970283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132589000-C-A

105970288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132588995-A-G

105970477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 132588803-A-G

105970483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 132588797-A-G

105970652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132588625-G-T

http://identifiers.org/hco/4/GRCh38#105970663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132588614-A-C

105970663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132588614-A-G

http://identifiers.org/hco/4/GRCh38#105970685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132588444-A-C

105970750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132588388-A-G

105970783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132588358-A-G

105970841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132588296-G-A

http://identifiers.org/hco/4/GRCh38#105970895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132588255-C-A

105970946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132588203-T-C

105970980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132588165-G-A

105971023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132588122-T-G

105971061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132588086-A-G

105971063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132588084-A-G

http://identifiers.org/hco/4/GRCh38#105971071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132588077-C-A

105971152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 132588001-G-A

105971152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 132588001-G-T

105971231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132587927-T-A

105971286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132587878-G-C

105971361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132587811-G-T

105971362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132587810-G-A

105971362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132587810-G-T

http://identifiers.org/hco/4/GRCh38#105971388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132587782-A-C

105971389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132587781-G-A

105971389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132587781-G-T

105971480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132587698-A-T

105971506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132587672-T-C

105971507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132587671-T-C

105971517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132587661-A-G

105971776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132587408-T-C

105971779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132587405-T-G

105972513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132586717-A-G

105972722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132586571-G-A

105972836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132586485-T-C

105972836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132586485-T-G

http://identifiers.org/hco/4/GRCh38#105973087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132586252-C-A

http://identifiers.org/hco/4/GRCh38#105973345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132586017-A-C

105975709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132584712-A-G

105976092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132584371-C-T

105976230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132584275-G-T

105976262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132584248-C-G

105976455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132584063-A-G

105976550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132583991-T-C

105976599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132583949-C-T

http://identifiers.org/hco/4/GRCh38#105976832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132583744-C-A

http://identifiers.org/hco/4/GRCh38#105977380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132583285-A-C

105978162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132582724-G-C

105978177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132582708-G-A

105978686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132582409-T-G

http://identifiers.org/hco/4/GRCh38#105978734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132582361-A-C

105978917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132582165-C-G

105978966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132582114-G-C

105978966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132582114-G-T

105979000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132582080-T-G

http://identifiers.org/hco/4/GRCh38#105979002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132582078-C-A

105979002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132582078-C-T

105979177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132581893-G-A

http://identifiers.org/hco/4/GRCh38#105988233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132580709-C-A

105988943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132579853-A-G

105989061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132579753-G-T

105989397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132579465-C-T

105989471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132579390-G-A

105989602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132579259-G-A

105989602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132579259-G-T

105989824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132579045-C-G

105989824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132579045-C-T

105989921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132578954-A-T

http://identifiers.org/hco/4/GRCh38#105989994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132578879-C-A

105990264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132578143-C-T

105990305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132578107-A-G

105990343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132578075-G-A

105990421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132578006-G-A

105990806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132577673-C-T

105990866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, undefined
orthologous variants: 132577613-C-T

105990921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132577557-G-C

105990923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132577555-A-G

105991178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132577318-A-G

105991248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132577252-T-G

105991545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132576949-C-G

105991663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132576840-G-A

105992061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132576576-G-A

105992172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132576497-C-T

105992176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132576493-T-C

105992495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132576288-C-G

105992831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132576003-G-A

105992895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132575935-C-G

105992970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132575857-C-T

105993016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132575769-T-C

105993044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132575744-A-G

105993087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132575702-A-G

105993589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132575323-C-G

105993710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132575243-G-C

105993758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132575194-C-G

105993758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132575194-C-T

105993841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132575120-G-T

http://identifiers.org/hco/4/GRCh38#105993955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132575020-A-C

105993955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132575020-A-T

105994286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132574761-G-A

105994324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132574723-G-A

105995773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132574278-G-A

105995877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132574149-G-C

105996176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132573841-T-C

105996260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132573759-G-A

http://identifiers.org/hco/4/GRCh38#105996500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132573546-A-C

105996862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132573264-T-C

105997010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132573148-G-A

105997010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132573148-G-C

105997235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132572916-A-G

105998291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron_variant, undefined
orthologous variants: 132571613-C-T

105998434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132571475-C-T

105998714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132571197-C-G

105998774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132571132-T-C

105999054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132570865-A-G

http://identifiers.org/hco/4/GRCh38#105999103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132570828-C-A

105999103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132570828-C-T

105999262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132570772-T-G

105999527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132570528-C-T

105999738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132570328-C-T

http://identifiers.org/hco/4/GRCh38#106000266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132569766-C-A

106000266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132569766-C-T

106000432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132569621-A-T

106000625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132569467-C-G

106000625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132569467-C-T

106000684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132569414-C-T

106001114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132568996-G-A

106001173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132568934-C-T

106001402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132568718-G-C

106001445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132568649-G-T

106001527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132568501-G-A

106001645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132568387-C-G

106001794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132568256-T-C

106001803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132568247-G-A

106001899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132568154-C-T

106001909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132568144-C-G

106001909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132568144-C-T

106001956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132568106-G-A

106001956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132568106-G-C

106002031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27405
most severe consequence: intron variant
orthologous variants: 132568022-G-A