46053877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85537817-T-A

46053877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85537817-T-C

http://identifiers.org/hco/22/GRCh38#46053943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85537883-C-A

46053943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85537883-C-T

46054017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85537943-G-A

46054017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85537943-G-T

46054073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85537980-A-G

http://identifiers.org/hco/22/GRCh38#46054110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85538009-C-A

46054110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85538009-C-G

46054110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85538009-C-T

46054115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85538014-C-T

46054121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85538029-C-T

http://identifiers.org/hco/22/GRCh38#46054127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85538036-C-A

46054127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85538036-C-G

46054127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85538036-C-T

46054129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85538038-A-T

46054130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85538039-G-A

46054130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85538039-G-T

46054132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85538041-G-A

46054132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85538041-G-T

46054141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85538054-G-A

46054141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85538054-G-C

46054141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85538054-G-T

46054168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85538082-A-G

46054168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85538082-A-T

46054182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85538101-G-A

46054182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85538101-G-C

46054182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85538101-G-T

http://identifiers.org/hco/22/GRCh38#46054197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85538116-C-A

46054197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85538116-C-G

46054197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85538116-C-T

46054228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85538154-G-A

46054228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85538154-G-C

46054228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85538154-G-T

46054337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85538239-T-A

46054337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85538239-T-C

46054337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85538239-T-G

46054471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85538369-G-A

http://identifiers.org/hco/22/GRCh38#46054562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85538459-C-A

46054562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85538459-C-G

46054562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85538459-C-T

46054581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85538478-G-A

46054581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85538478-G-T

46054713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85538616-A-G

http://identifiers.org/hco/22/GRCh38#46054714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85538617-C-A

46054778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85538669-A-G

http://identifiers.org/hco/22/GRCh38#46054903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85538790-C-A

46054903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85538790-C-G

46054909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85538794-G-A

46054946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85538812-C-T

46054952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 85538818-G-T

46055035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85538881-G-C

46055105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85538952-T-C

http://identifiers.org/hco/22/GRCh38#46055138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85538986-C-A

46055138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85538986-C-T

46055334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85539168-C-T

46055520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85539318-C-T

http://identifiers.org/hco/22/GRCh38#46055534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85539336-C-A

46055534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85539336-C-T

46055545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85539347-C-T

46055548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85539350-G-A

46055548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85539350-G-C

http://identifiers.org/hco/22/GRCh38#46055551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85539353-C-A

46055551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85539353-C-T

46055560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85539362-C-G

46055567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85539384-A-G

46055606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85539436-C-T

46055615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85539445-A-G

46055622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85539464-A-G

46055629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85539474-C-T

46055901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85539766-G-A

46055901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85539766-G-T

http://identifiers.org/hco/22/GRCh38#46055902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85539767-C-A

46055902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85539767-C-T

http://identifiers.org/hco/22/GRCh38#46055911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85539776-C-A

46055911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85539776-C-T

46055986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85539847-T-C

46056018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85539894-A-G

46056019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85539895-G-T

http://identifiers.org/hco/22/GRCh38#46056240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85540118-C-A

46056240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85540118-C-T

46056267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85540145-G-A

46056267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85540145-G-T

46056400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85540283-C-T

46056517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 85540388-T-C

46056897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85540749-G-A

46056937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85540797-C-G

46056937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85540797-C-T

46057006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85540856-A-G

46057113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85540971-G-T

46057223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85541097-G-A

46057249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85541127-T-A

46057355-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85541221-T-G

46057356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85541222-G-T

46057372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85541236-C-T

46058037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85541849-G-T

46058041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85541853-T-C

46058135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85541959-C-T

http://identifiers.org/hco/22/GRCh38#46058307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85542094-A-C

46058626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85542386-C-G

46058626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85542386-C-T

46058627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85542387-G-A

46058869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85542599-C-T

46059012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85542744-C-G

46059012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85542744-C-T

46059041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85542760-G-A

46059105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85542808-C-G

46059369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85543056-G-A

46059756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85543401-T-C

46059980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85543605-A-T

46060012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85543636-G-A

46060088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85543711-G-A

46060373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85544017-A-G

46060427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85544064-A-T

46060595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85544227-T-C

46060595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85544227-T-G

46061051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85544599-G-A

46061136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85544703-G-C

46061258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85544930-G-T

46061308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85544971-G-C

46061747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85545383-G-T

46061765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85545412-G-T

46061788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85545435-C-T

46061836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85545499-G-A

46061836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85545499-G-C

46061903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85545579-G-C

http://identifiers.org/hco/22/GRCh38#46061930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85545629-C-A

46062000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85545729-G-A

46062070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85545825-T-G

46062082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85545837-G-T

46062083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85545838-C-T

46062281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85546007-T-C

46062329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85546060-G-A

46062329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85546060-G-C

46062824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85546499-A-G

46062866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85546536-T-G

46063037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85546690-G-T

http://identifiers.org/hco/22/GRCh38#46063055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85546705-C-A

46063104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85546756-T-C

46063207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85546812-T-A

46063207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85546812-T-C

46063297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85546906-C-T

46063364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85546967-A-G

46063869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85547463-G-A

46064011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85547591-G-A

46064669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85548122-T-C

46064845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85548291-C-G

46064921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85548367-C-T

46064922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85548368-G-A

46064925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85548371-T-C

46064933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85548379-C-T

http://identifiers.org/hco/22/GRCh38#46064942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85548388-A-C

46064942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85548388-A-G

46064973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85548465-A-G

46065154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85548647-G-A

46065211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85548704-C-T

46066406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85550355-A-T

46066407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85550356-T-C

46066425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85550381-C-T

46066644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85550607-G-T

46067997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85552122-G-A

46067997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85552122-G-C

http://identifiers.org/hco/22/GRCh38#46068003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85552128-C-A

46068003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85552128-C-T

46068129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85552260-G-T

46068487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85552641-C-T

46068579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85552734-C-T

46068725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85552890-G-A

46069263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85553371-T-C

46069717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85553611-T-C

46069750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85553633-C-T

http://identifiers.org/hco/22/GRCh38#46069810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85553696-C-A

46069810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85553696-C-T

46069834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85553726-C-T

46070110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85554005-C-T

46070138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85554033-C-G

http://identifiers.org/hco/22/GRCh38#46071486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85555237-A-C

46071541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85555298-G-A

http://identifiers.org/hco/22/GRCh38#46071620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85555376-C-A

46071620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85555376-C-G

46071620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85555376-C-T

46071802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85555558-G-A

46071820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85555576-A-G

46071820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85555576-A-T

46071923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85555679-G-A

http://identifiers.org/hco/22/GRCh38#46072029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85555774-C-A

46072206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85555944-G-C

46072397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85556109-C-T

46072989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85556621-G-A

46072989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85556621-G-T

46072998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85556630-T-G

46073040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85556672-G-A

46073345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85556998-G-A

46074242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85557972-G-A

46074316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85558048-G-C

46074375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85558105-C-T

46074717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85558347-A-G

46074725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85558356-G-T

46074813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85558432-C-T

46074969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85558549-A-G

46075136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85558676-G-A

46075203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85558752-C-T

46075703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85559254-A-G

46076005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85559504-T-C

46076084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85559539-A-T

http://identifiers.org/hco/22/GRCh38#46076118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85559574-A-C

46076577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85559989-G-C

46076642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85560052-G-A

46076779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85560177-A-G

46076959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85560364-C-G

46077157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85560600-G-C

46077202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85560647-G-A

46077202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85560647-G-T

46077287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85560729-G-A

46077287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85560729-G-T

46077432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85560871-A-G

46077525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85560967-A-G

46077566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85561008-G-C

46077651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85561138-A-G

46077771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85561255-C-T

46077788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85561270-G-A

46077788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85561270-G-T

46077878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85561343-A-G

46078105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85561548-A-G

46079077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85562475-C-T

46079364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85562731-C-T

46079373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85562740-G-A

46079373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85562740-G-T

46079507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85562853-G-A

http://identifiers.org/hco/22/GRCh38#46080109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85563407-C-A

46080109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85563407-C-T

46080169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85563467-G-A

46080169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85563467-G-T

46080184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85563482-T-C

46080195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85563498-T-C

http://identifiers.org/hco/22/GRCh38#46080218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85563521-A-C

http://identifiers.org/hco/22/GRCh38#46080276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85563580-C-A

46080276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85563580-C-T

46080292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85563596-G-A

http://identifiers.org/hco/22/GRCh38#46080293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85563597-C-A

46080293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85563597-C-T

http://identifiers.org/hco/22/GRCh38#46080406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85563718-C-A

46080415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85563726-G-A

46080415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85563726-G-T

46080478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85563791-G-T

http://identifiers.org/hco/22/GRCh38#46080521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85563829-C-A

46080521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85563829-C-T

http://identifiers.org/hco/22/GRCh38#46080577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85563885-C-A

46080577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85563885-C-T

http://identifiers.org/hco/22/GRCh38#46080693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85563990-C-A

46080693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85563990-C-T

46080745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85564047-T-C

46080777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85564101-G-A

46080777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85564101-G-T

46080918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85564242-G-A

46080966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85564285-G-A

46081145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85564445-G-A

http://identifiers.org/hco/22/GRCh38#46081301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85564615-A-C

46081301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85564615-A-G

46081602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85564930-G-A

46082070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85565375-A-G

46082070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85565375-A-T

46082263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85565572-G-A

46082678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85565980-T-C

46082699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85566004-C-T

46082779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85566078-T-C

46082782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85566081-C-T

http://identifiers.org/hco/22/GRCh38#46083059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85566428-C-A

46083059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85566428-C-T

46083242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85566698-G-A

46083242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85566698-G-C

46083776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85567352-C-T

46083851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85567425-G-C

46083851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85567425-G-T

46083935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85567506-C-T

http://identifiers.org/hco/22/GRCh38#46084095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85567643-C-A

46084095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85567643-C-T

46084427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85567898-A-G

46084594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85568041-C-G

46084594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85568041-C-T

46084614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85568060-G-A

46084760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85568216-G-A

46084930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85568393-C-T

http://identifiers.org/hco/22/GRCh38#46085404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85568791-A-C

46085404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85568791-A-G

46085462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85568840-C-T

46085677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85569088-C-T

46085715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85569127-C-T

46085849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85569213-G-A

46085849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85569213-G-T

46085855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85569219-G-A

46085855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85569219-G-T

http://identifiers.org/hco/22/GRCh38#46085866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85569228-C-A

46085866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85569228-C-T

46085867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85569229-A-G

46085986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85569348-G-A

46085986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85569348-G-C

46086033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85569385-C-G

http://identifiers.org/hco/22/GRCh38#46086096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85569464-C-A

46086096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85569464-C-G

http://identifiers.org/hco/22/GRCh38#46086129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85569498-C-A

46086129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85569498-C-T

46086155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85569539-G-C

46086157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85569544-G-A

46086157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85569544-G-T

46086190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85569577-G-T

46086247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85569633-C-T

46086307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85569700-T-C

46086729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85570100-C-T

46086869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85570237-G-T

46086967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85570273-G-T

46087053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85570350-C-T

46087318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85570605-G-A

46087318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85570605-G-C

46087399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85570688-G-A

46087401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85570690-A-G

46087480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85570766-C-T

46087955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85571201-G-A

46087986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85571230-C-T

46088027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85571270-G-A

46088118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85571372-G-A

46088118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85571372-G-C

46088118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85571372-G-T

http://identifiers.org/hco/22/GRCh38#46088135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85571382-A-C

46088236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85571480-G-A

http://identifiers.org/hco/22/GRCh38#46088264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85571508-C-A

46088290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85571534-G-A

46088384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85571654-G-A

46088439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85571712-G-A

46088515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85571784-G-C

46088515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85571784-G-T

46088547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85571832-C-T

46088580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85571870-A-G

46088587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85571875-T-C

46088598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85571889-G-C

46088598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85571889-G-T

46088612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85571902-G-T

46088637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85571926-G-T

46088656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85571937-A-G

46088901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85572116-T-A

46089457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85572510-G-C

46089573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85572614-G-A

46089616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85572616-G-A

46089633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85572633-C-T

46089718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85572687-G-A

http://identifiers.org/hco/22/GRCh38#46089800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85572760-C-A

46089917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85572873-T-A

46090003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85572943-T-G

46090294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85573243-G-T

46091922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85574167-G-A

46092249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85574482-G-A

46092603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85574808-C-T

46092624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85574829-C-G

46092664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85574867-G-A

46093133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85575290-T-C

46093136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85575293-G-A

46097092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85577016-C-T

46097162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85577082-C-G

46097162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85577082-C-T

46097277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85577186-G-A

46097777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85577586-T-C

46097786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85577595-G-A

46097786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85577595-G-T

46097833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85577639-G-T

46097838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85577644-G-A

46097861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85577667-T-C

46097861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85577667-T-G

46097943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 85577753-G-A

46097973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 85577783-G-A

46097995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 85577805-G-T

http://identifiers.org/hco/22/GRCh38#46098055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85577858-C-A

46098055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85577858-C-G

http://identifiers.org/hco/22/GRCh38#46098132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85577962-C-A

http://identifiers.org/hco/22/GRCh38#46098140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85577969-C-A

http://identifiers.org/hco/22/GRCh38#46098150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85577979-C-A

46098150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85577979-C-G

http://identifiers.org/hco/22/GRCh38#46098155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85577984-C-A

46098155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85577984-C-T

46098158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85577987-G-T

46098363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85578999-C-T

46098471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85579095-T-C

46098518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85579143-C-G

http://identifiers.org/hco/22/GRCh38#46098534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85579159-C-A

46098948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85579418-C-T

46099248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85579665-C-T

46099278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85579695-C-T

46099328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85579743-C-T

46099447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85579844-A-G

46099451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85579848-G-A

46099702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85580004-C-G

46099943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85580196-G-A

46099948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85580201-G-C

46099984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85580229-C-G

46100036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85580282-G-A

46100036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85580282-G-T

46100196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85580424-C-G

46100411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85580580-G-T

46100495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85580644-G-A

46103000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85582961-C-T

46103038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85583001-C-G

46103039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85583002-G-A

46103039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85583002-G-T

46103093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85583056-G-A

46103093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85583056-G-T

46103164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85583111-C-T

46103186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 85583141-A-G

46103197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85583152-G-A

46103316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85583285-G-A

46103316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85583285-G-T

46103426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85583420-A-G

46103638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85583579-C-T

46103773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85583746-C-T

46103797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85583770-G-T

46104026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85583964-G-A

46104026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85583964-G-C

46104467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85584403-C-T

46104659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85584614-A-G

http://identifiers.org/hco/22/GRCh38#46104681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85584641-A-C

http://identifiers.org/hco/22/GRCh38#46104793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85584828-C-A

46104805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85584840-C-G

46104911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85584923-C-G

46104917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85584929-T-G

46104928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85584940-T-C

46104951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85584970-C-T

46104978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85584994-C-T

46105064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585074-G-A

46105204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585202-G-A

http://identifiers.org/hco/22/GRCh38#46105296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85585272-C-A

46105296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585272-C-T

46105324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585294-A-T

46105328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585298-C-T

46105330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585300-G-A

46105330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585300-G-T

46105345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585314-G-A

46105345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585314-G-T

http://identifiers.org/hco/22/GRCh38#46105360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85585327-C-A

46105360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585327-C-T

http://identifiers.org/hco/22/GRCh38#46105720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85585583-C-A

46105720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585583-C-T

http://identifiers.org/hco/22/GRCh38#46105746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85585608-C-A

46105746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585608-C-G

46105746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585608-C-T

46105780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585640-G-A

46105780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585640-G-C

46105783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585641-C-T

46105834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585691-G-T

46105843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585699-T-C

46105856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585710-G-T

46105859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585713-T-G

46105862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585716-C-T

46105866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585717-A-G

46105876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585727-T-C

46105906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585752-G-A

46105906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585752-G-T

46106014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585834-G-A

46106014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585834-G-T

46106114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585933-G-C

46106114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585933-G-T

46106157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585977-G-A

46106157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585977-G-T

http://identifiers.org/hco/22/GRCh38#46106173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85585993-C-A

46106173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85585993-C-G

46106201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85586021-C-T

46106668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85586231-A-T

46106954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85586425-C-T

46107051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85586523-C-T

46107115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85586610-G-A

46107165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85586657-G-A

46107165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85586657-G-C

46107181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85586674-C-T

46107447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85586943-A-G

46107582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85587049-A-T

46107589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85587056-G-A

46107729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85587170-C-T

46107738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85587179-C-G

46107780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85587216-C-T

http://identifiers.org/hco/22/GRCh38#46107859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85587292-A-C

46107859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85587292-A-G

46108062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85587426-C-T

46108151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85587501-G-C

46108211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85587559-G-A

46108299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85587678-A-G

46108372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85587744-C-T

46108392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85587764-G-A

46108480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85587835-C-G

46108548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85587934-G-A

46108610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85588008-C-T

http://identifiers.org/hco/22/GRCh38#46109118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85588301-C-A

46109118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85588301-C-T

46109152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85588334-G-T

46109173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85588361-G-A

46109173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85588361-G-T

46109309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85588481-C-T

46109322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85588494-G-T

46109337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85588507-C-T

46109402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85588562-G-T

46109406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85588566-G-A

46109406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85588566-G-C

46109465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85588622-T-C

46109610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85588725-T-C

http://identifiers.org/hco/22/GRCh38#46109690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85588807-C-A

46109690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85588807-C-T

46109793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85588859-G-T

46109954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589017-T-A

46109977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589037-G-T

46110030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589086-G-A

46110030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589086-G-C

46110030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589086-G-T

46110092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589126-C-G

http://identifiers.org/hco/22/GRCh38#46110128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85589150-C-A

46110161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589184-G-A

http://identifiers.org/hco/22/GRCh38#46110162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85589185-C-A

46110162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589185-C-T

46110174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589197-G-A

46110174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589197-G-T

46110221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589254-G-A

46110221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589254-G-T

46110228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589256-G-A

46110312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589316-G-T

http://identifiers.org/hco/22/GRCh38#46110387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85589372-C-A

http://identifiers.org/hco/22/GRCh38#46110404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85589387-C-A

46110404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589387-C-T

46110444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589397-G-A

46110444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589397-G-T

46110530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589436-T-C

46110530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589436-T-G

http://identifiers.org/hco/22/GRCh38#46110651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85589595-C-A

46110651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589595-C-G

46110894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589823-G-T

46110923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589841-G-T

46110982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589894-G-A

46110982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589894-G-T

46111003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589918-C-T

46111004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589919-G-A

46111004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589919-G-T

46111016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589931-G-A

46111055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589969-G-A

46111055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85589969-G-T

http://identifiers.org/hco/22/GRCh38#46112009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85590192-C-A

46112009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590192-C-T

http://identifiers.org/hco/22/GRCh38#46112011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85590194-C-A

http://identifiers.org/hco/22/GRCh38#46112063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85590242-C-A

http://identifiers.org/hco/22/GRCh38#46112145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85590323-C-A

46112145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590323-C-T

46112159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590340-G-T

46112203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590384-T-A

46112203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590384-T-G

46112219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590400-G-A

46112219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590400-G-C

46112219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590400-G-T

http://identifiers.org/hco/22/GRCh38#46112234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85590413-A-C

46112234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590413-A-G

46112282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590456-G-A

46112282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590456-G-T

46112319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590496-G-A

46112319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590496-G-T

46112459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590567-G-T

46112479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590591-T-C

http://identifiers.org/hco/22/GRCh38#46112555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85590643-C-A

46112555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590643-C-T

46112573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590660-G-A

46112573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590660-G-T

46112611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590699-G-T

http://identifiers.org/hco/22/GRCh38#46112617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85590705-C-A

46112617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590705-C-T

46112868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590930-G-A

46112868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590930-G-T

http://identifiers.org/hco/22/GRCh38#46112920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85590960-C-A

46112920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590960-C-T

46112949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85590989-A-G

http://identifiers.org/hco/22/GRCh38#46113018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85591033-C-A

46113026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85591041-T-C

46113039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85591055-G-A

46113039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85591055-G-T

46113124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85591112-G-A

46113124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85591112-G-T

http://identifiers.org/hco/22/GRCh38#46113165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85591114-C-A

http://identifiers.org/hco/22/GRCh38#46113174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85591123-A-C

46113174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85591123-A-G

46113174-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85591123-A-T

46113183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85591132-G-A

46113183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85591132-G-T

46113197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85591145-G-A

46113197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85591145-G-T

46113351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85591220-T-C

http://identifiers.org/hco/22/GRCh38#46113393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85591246-C-A

46113393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85591246-C-T

46113402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85591255-T-C

http://identifiers.org/hco/22/GRCh38#46113451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85591298-C-A

46113451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85591298-C-T

46113482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85591337-T-C

46113523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85591375-A-G

46113554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85591409-G-A

46113554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85591409-G-T

http://identifiers.org/hco/22/GRCh38#46113575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85591428-C-A

46113575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85591428-C-T

46113785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85591620-G-A

46113785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37189
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 85591620-G-T