219686067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185391398-A-G

219689702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185386804-G-T

219689746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185386553-T-C

219689770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185386529-G-T

219690054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185386248-A-G

219690262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185386049-A-G

http://identifiers.org/hco/1/GRCh38#219690406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185385921-A-C

219690799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185385521-G-A

219690935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185385385-C-T

219691746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185384892-C-T

219691806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185384838-A-G

219692265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185384424-A-T

219692341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185384350-A-G

219692348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185384343-A-G

219692351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185384337-G-A

219692362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185384326-A-G

219692672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185383865-G-A

219692672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185383865-G-T

219692833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185383735-G-C

219692960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185383614-T-C

219693051-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185383548-A-T

http://identifiers.org/hco/1/GRCh38#219693170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185383421-A-C

219693234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185383357-T-C

219693673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185382629-C-T

219694036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185382272-T-C

219694288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185382037-T-A

219694304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185382021-C-G

219694304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185382021-C-T

219696789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185381054-T-C

219696897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185380639-A-T

http://identifiers.org/hco/1/GRCh38#219699200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185379432-C-A

219699330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185379290-A-G

219699445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185379041-A-G

219699867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185378597-A-G

219699942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185378522-A-T

219700031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185378438-T-C

http://identifiers.org/hco/1/GRCh38#219700065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#185378404-A-C

219700178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185378312-C-T

219700553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185378133-T-C

219700694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185378003-T-C

219700699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185377998-G-C

http://identifiers.org/hco/1/GRCh38#219700719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185377983-A-C

http://identifiers.org/hco/1/GRCh38#219700945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185377786-C-A

http://identifiers.org/hco/1/GRCh38#219700956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185377775-A-C

219701077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185377130-G-A

219701320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185376885-G-A

219701428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185376774-C-T

219701473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185376734-A-G

219701687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185376518-A-G

219701785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185376416-A-G

219701812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185376390-C-T

219702041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185376154-C-T

http://identifiers.org/hco/1/GRCh38#219702216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185376019-A-C

http://identifiers.org/hco/1/GRCh38#219702350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185375901-A-C

219702354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185375897-G-A

219702354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185375897-G-C

http://identifiers.org/hco/1/GRCh38#219702421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185375815-C-A

219702421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185375815-C-T

219702439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185375797-A-G

219702457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185375779-T-A

219702735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185375287-T-C

219702736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185375286-G-A

219702816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185375208-G-A

219702824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185375178-A-G

219703183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185374887-T-A

219703392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185374712-A-G

219703421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185374680-A-G

219703683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185374429-T-C

219703786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185374333-A-T

http://identifiers.org/hco/1/GRCh38#219708543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185374015-C-A

219708543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185374015-C-T

219708565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185374005-T-C

219708720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185373852-G-C

219708774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185373798-A-G

219708863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185373699-C-T

219708914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185373649-C-T

219708952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185373618-C-T

219708989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185373583-T-C

219709142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185373426-C-T

219709157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185373411-G-A

219709244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185373329-A-G

219709581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185372969-A-T

219709601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185372958-C-T

219709623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185372936-C-G

219709944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185372681-T-C

219709984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185372641-G-A

http://identifiers.org/hco/1/GRCh38#219710028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185372601-A-C

219710051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185372579-G-T

219710266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185372368-G-T

219710337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185372298-T-G

219710444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185372194-T-C

219710488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185372150-A-G

219710497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185372142-T-C

219710790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185371880-G-A

219710902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185371788-C-T

219710911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185371778-G-T

219712492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185369641-C-T

219712658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185369473-T-C

219713054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185368666-A-G

219713433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185367543-A-G

http://identifiers.org/hco/1/GRCh38#219713502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185367481-A-C

219713502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185367481-A-G

219713633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185367376-T-A

http://identifiers.org/hco/1/GRCh38#219713664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185367344-A-C

219713938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185367104-A-G

219714042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185367043-A-G

219714148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185366942-G-T

219714535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185366545-T-C

219714683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185366405-G-A

219714777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185366316-C-T

219714789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185366307-T-G

219714963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185366139-T-C

219714965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185366137-C-T

219714966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185366136-C-T

219715045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185365390-G-C

219715096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185365341-T-A

219715269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185365173-G-A

219715296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185365146-T-C

http://identifiers.org/hco/1/GRCh38#219715326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185365116-C-A

219715334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185365108-A-G

219715348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185363983-T-A

http://identifiers.org/hco/1/GRCh38#219715384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185363947-C-A

219715384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185363947-C-T

219715506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185363845-A-G

219715585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185363765-A-G

219715684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185363684-A-G

219715688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185363680-C-T

219715689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185363679-T-C

219715700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185363668-T-C

219715724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185363644-A-T

219715737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185363631-T-A

219716023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185363360-T-A

http://identifiers.org/hco/1/GRCh38#219716236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185363088-A-C

219741339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185361375-C-G

219741349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185361365-G-A

219741352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185361362-C-T

219741355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185361359-T-A

219741707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185361110-A-T

219741948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185360884-T-A

219742445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185353376-G-A

219742569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185353252-G-T

219742707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185353134-C-T

http://identifiers.org/hco/1/GRCh38#219742716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185353125-C-A

219742732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185353112-T-G

219742787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185353058-C-G

http://identifiers.org/hco/1/GRCh38#219743130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185352815-C-A

219743169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185352783-C-T

219743173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185352779-T-G

http://identifiers.org/hco/1/GRCh38#219743175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185352778-C-A

219743175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185352778-C-T

219743570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185352713-C-G

219743649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185352635-C-T

219743678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185352609-G-C

219743721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185352568-A-G

219743739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185352547-T-C

219743839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185352447-T-G

http://identifiers.org/hco/1/GRCh38#219743850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185352436-C-A

219743850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185352436-C-T

219744099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185351868-G-A

http://identifiers.org/hco/1/GRCh38#219744142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185351826-C-A

219744775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185351599-A-G

219744841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185351533-C-T

219744873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185351501-T-G

219744906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185351472-T-C

219744907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185351471-G-A

219744907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185351471-G-C

219744913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185351465-A-T

219744933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185351445-A-T

219745049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185351325-T-C

219745493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185350922-G-C

219745520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185350895-G-T

219745860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185350569-G-A

219745895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185350535-G-A

219745895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185350535-G-T

219745965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185350473-T-C

219746005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185350437-T-G

219746029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185350413-T-A

219746166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185350280-C-G

219746179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185350267-T-C

219746435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185350022-C-T

219746806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185349616-A-G

219746970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185349457-G-A

219746970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185349457-G-C

219747725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185349050-C-G

219747810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185348977-G-A

219747847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185348940-G-A

219748166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185348651-A-G

http://identifiers.org/hco/1/GRCh38#219748389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185348433-C-A

219748393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185348429-A-T

219748556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185348266-T-C

219748883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185347963-T-A

219748883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185347963-T-C

219748883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185347963-T-G

219748891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185347951-G-A

219748891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185347951-G-T

http://identifiers.org/hco/1/GRCh38#219748926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185347922-C-A

219749069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185347783-T-C

219749335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185347491-A-G

219749353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185347452-C-T

219753664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185346921-G-C

219753664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185346921-G-T

219753668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185346917-A-T

219753706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185346879-T-C

219754161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185346472-A-G

219754251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185346391-C-T

219754352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185346294-G-A

219754400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185346248-G-T

219754475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185346186-A-G

219754793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185345929-G-A

219754793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185345929-G-C

219754795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185345927-G-A

219754795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185345927-G-T

219755073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185345495-A-G

219755170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185345404-C-T

219755187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185345388-T-A

219755187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185345388-T-C

219755196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185345379-G-A

219755455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185345111-A-G

219755530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185345037-G-A

http://identifiers.org/hco/1/GRCh38#219755610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185344962-C-A

219755970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185344893-T-A

219755970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185344893-T-G

219756096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185344818-A-G

219756248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185344669-A-G

http://identifiers.org/hco/1/GRCh38#219756297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185344616-C-A

219756297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185344616-C-G

219756341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185344561-G-A

219756341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185344561-G-T

219756343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185344559-T-A

219756343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185344559-T-C

219756343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185344559-T-G

219756351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185344552-G-A

219756436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185344464-A-G

219756492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185344408-A-G

219756626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185344111-G-A

219756802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185343900-T-C

219756892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185343820-A-T

http://identifiers.org/hco/1/GRCh38#219756936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185343777-C-A

219757559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185343612-T-C

219757745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185343435-A-G

219758279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185342904-T-C

219758441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185342761-T-C

219758487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185342715-A-G

219758505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185342707-A-G

219759898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185340725-G-A

219759942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185340671-T-A

219760013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185340631-T-G

219760038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185340606-T-C

219760100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185340557-A-G

http://identifiers.org/hco/1/GRCh38#219760380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185340041-C-A

219760380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185340041-C-T

http://identifiers.org/hco/1/GRCh38#219763316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185338093-C-A

219763316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185338093-C-G

219763316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185338093-C-T

219763372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185338034-G-A

219763402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185338003-T-C

219763423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185337982-A-G

219763474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185337931-A-G

219763598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185337794-T-A

219763920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185337270-G-C

219763986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185337193-G-C

219764212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185336985-T-A

219764276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185336918-A-T

219765018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185336232-G-A

219765018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185336232-G-T

219765019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185336231-T-C

219765024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185336226-A-G

http://identifiers.org/hco/1/GRCh38#219765067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185336183-C-A

219769925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185331055-T-C

219769996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185330985-G-T

219770154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185330833-G-A

219770196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185330790-T-C

219770212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185330774-A-G

219770343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185330643-C-T

219770421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185330565-A-T

219770444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185330542-T-C

219770995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185329359-A-G

219771246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185329118-C-T

219771252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185329112-G-A

219771252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185329112-G-T

http://identifiers.org/hco/1/GRCh38#219772696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185327634-A-C

219772942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185327409-T-C

219778890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185325795-G-A

219778918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185325767-A-G

219779295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185325356-G-A

219779358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185325295-G-C

219779488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185325143-C-T

219780916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185323170-C-T

219781144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185322767-G-A

219784156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185320939-A-G

219784156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185320939-A-T

219784288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185320818-G-A

219784393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185320718-G-A

219784494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185320628-T-C

219784518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185320603-A-G

219784563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185320558-C-T

219784569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185320552-C-G

219784569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185320552-C-T

219785046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185320090-C-G

http://identifiers.org/hco/1/GRCh38#219785415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185319727-A-C

219785426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185319715-G-C

219785426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185319715-G-T

219785591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185319541-T-C

219785802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185319370-C-T

219785867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185319304-T-C

http://identifiers.org/hco/1/GRCh38#219785970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185319222-A-C

219786056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185319092-C-G

219786147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185319016-A-G

219786211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185318957-T-A

219786256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185318912-T-C

219786268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185318898-A-G

219786347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185318818-G-A

219786355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185318810-C-T

http://identifiers.org/hco/1/GRCh38#219788144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185311034-A-C

219788178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185311007-G-A

219788320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185310867-G-A

http://identifiers.org/hco/1/GRCh38#219788412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185310819-C-A

219788412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185310819-C-T

219788649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185310573-C-T

219788813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185310397-C-T

219788885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185310314-A-G

219789033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185310162-A-G

219789035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185310160-C-T

219789098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185310112-A-G

219789098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185310112-A-T

219789133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185310086-T-G

219789351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185309194-G-T

219790089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185308768-A-G

219790359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: non coding transcript exon variant
orthologous variants: 185308520-T-A

219790373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: non coding transcript exon variant
orthologous variants: 185308506-G-A

219790373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: non coding transcript exon variant
orthologous variants: 185308506-G-T

219790441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: non coding transcript exon variant
orthologous variants: 185308463-G-C

http://identifiers.org/hco/1/GRCh38#219790555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185308347-C-A

219790577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185308324-G-T

219790580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185308319-T-C

219790598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185308301-G-A

219790598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185308301-G-T

219790602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185308297-G-A

219790708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185308196-C-G

219790721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185308181-C-T

219790874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185307462-C-T

219790894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185307442-G-A

219790935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185307401-G-A

219791146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185307180-T-A

219791146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185307180-T-C

219791171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185307154-G-C

219791171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185307154-G-T

219791173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185307152-C-T

http://identifiers.org/hco/1/GRCh38#219791260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185307088-A-C

219791355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 185306996-A-G

219791485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 185306868-G-A

219791485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 185306868-G-C

219791596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: non coding transcript exon variant
orthologous variants: 185306753-G-T

219791613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: non coding transcript exon variant
orthologous variants: 185306735-G-T

http://identifiers.org/hco/1/GRCh38#219791620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185306728-C-A

http://identifiers.org/hco/1/GRCh38#219791665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185306689-C-A

219791665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: non coding transcript exon variant
orthologous variants: 185306689-C-T

219791793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: non coding transcript exon variant
orthologous variants: 185306599-A-G

219791885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: non coding transcript exon variant
orthologous variants: 185306166-T-A

http://identifiers.org/hco/1/GRCh38#219792122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185305930-C-A

219792129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185305923-T-G

219792203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185305834-T-C

219792621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 185305379-A-G

219792697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 185305303-T-C

219792796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 185305204-A-G

219792815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 185305187-C-G

219793105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185304899-C-T

219795009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185304782-C-T

219795206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185304607-G-A

219795210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185304603-G-T

219795395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185304419-G-A

219795517-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185304294-T-A

219795628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185304187-A-T

219795903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185303914-G-A

219796063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185303828-T-A

219796063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185303828-T-C

219796101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185303791-T-C

219797085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185303365-A-T

219797243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185303223-A-G

219797678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185302502-C-G

219797763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185302427-G-A

219797926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185294948-G-A

219798145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185294711-C-T

219799938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185293607-G-A

219799943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185293598-G-A

219800022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185293520-G-C

219800029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185293517-C-G

http://identifiers.org/hco/1/GRCh38#219800076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185293473-A-C

219800091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185293458-T-C

219800134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185293418-T-C

219800824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185292704-A-G

219801005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185292550-T-A

219801005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185292550-T-C

219801074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185292485-G-A

219801140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185292418-A-T

219801473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185292090-G-C

219801787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185291777-G-A

http://identifiers.org/hco/1/GRCh38#219801793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185291771-A-C

219801828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185291736-G-A

219802694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185290292-G-C

http://identifiers.org/hco/1/GRCh38#219802760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185290221-C-A

219802900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185290054-C-G

219802962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185289993-G-A

219802975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185289980-C-T

219802987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185289968-C-T

219803199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185289067-C-T

219803409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185288769-T-C

219803640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185288568-G-A

219803839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185288382-T-A

219804071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185287529-G-A

http://identifiers.org/hco/1/GRCh38#219804102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185287498-C-A

219804102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185287498-C-G

219804182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185287415-G-A

219804358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185287245-A-G

219804638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185286819-A-G

219804845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185286135-C-G

219804877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185286102-T-C

219805280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185285721-C-T

219805527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185285207-G-A

219805597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185285137-A-G

219805931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185285025-C-G

219806168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185284777-A-G

219806230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185284715-T-C

http://identifiers.org/hco/1/GRCh38#219806638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185283402-C-A

http://identifiers.org/hco/1/GRCh38#219806866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185283168-C-A

219806878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185283156-C-T

219806934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185283100-A-T

219807037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185283009-A-G

219807264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185282793-T-A

219808105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185281561-G-T

219808408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185281268-T-A

219811142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185280932-C-T

219811157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185280921-C-T

219811158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185280920-A-G

219811402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185280556-G-C

219811437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185280515-C-T

219811438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185280514-A-T

219811445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185280507-G-A

219811460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185280494-C-T

219812508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185279017-G-C

219812640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185278858-G-C

219812821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185278643-A-T

219812846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185278611-G-A

219813003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185278442-T-A

219813254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185278207-G-A

219813555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185277918-A-G

219813799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185277687-C-T

219813801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185277685-T-C

219817792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185271645-C-T

219817859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185271575-C-T

219818009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185271415-T-A

219818011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185271413-C-G

219818117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185271308-G-A

219818207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185271219-C-T

219818368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185271062-T-C

219818442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185271017-T-C

219819227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185270434-T-A

219819413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185270285-C-T

219819438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185270247-C-G

219819438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185270247-C-T

219819439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185270246-G-A

219819439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185270246-G-C

219819572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185270115-T-C

219819654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185270032-C-T

http://identifiers.org/hco/1/GRCh38#219819724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185269958-A-C

219819724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185269958-A-G

219819724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185269958-A-T

219820136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185269205-A-G

219820408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185268944-T-C

http://identifiers.org/hco/1/GRCh38#219820482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185268876-C-A

219820540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185268819-C-G

219820649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185268723-T-C

219820805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185268597-A-G

219820806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185268596-A-G

219820857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185268547-C-G

219820911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185268507-G-A

219821313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185267930-G-A

219821705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185267482-C-G

219821758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185267430-G-C

219822318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185266887-G-A

219822318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185266887-G-C

http://identifiers.org/hco/1/GRCh38#219822319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185266886-C-A

219822319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185266886-C-T

219822458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185266747-C-T

219822598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: non coding transcript exon variant
orthologous variants: 185266607-G-T

http://identifiers.org/hco/1/GRCh38#219822693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185266516-C-A

219822963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185266262-G-A

219823047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185266179-T-A

219823807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185265120-T-A

219823807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185265120-T-G

219823885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185265069-T-C

219823999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185264964-G-A

219824660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185264048-A-G

219825101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185263876-C-G

219825101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185263876-C-T

http://identifiers.org/hco/1/GRCh38#219825107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185263870-C-A

http://identifiers.org/hco/1/GRCh38#219825114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185263863-C-A

219825412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185263668-C-T

http://identifiers.org/hco/1/GRCh38#219825478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185263601-A-C

219825562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185263486-T-C

219826479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185256275-T-C

219826537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185256208-A-T

219826705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185256077-G-A

219835732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185252684-A-G

http://identifiers.org/hco/1/GRCh38#219835736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185252680-A-C

219836068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185252365-G-A

http://identifiers.org/hco/1/GRCh38#219836188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185252272-C-A

219836266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185252206-C-T

http://identifiers.org/hco/1/GRCh38#219837913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185249986-C-A

219837913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185249986-C-T

219838135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185249082-T-G

219838199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185249018-A-G

219838341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185248909-T-C

219838530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185248379-C-T

219838549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185248364-G-A

219838643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185248272-C-T

219838674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185248242-T-A

219838677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185248239-C-T

219858806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185241816-G-A

219858831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185241790-T-A

219858831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185241790-T-C

219858833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185241788-C-T

http://identifiers.org/hco/1/GRCh38#219859055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185241582-A-C

219859084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185241557-C-T

219859154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185241482-G-A

219871851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185240100-T-C

219871869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185240083-A-T

http://identifiers.org/hco/1/GRCh38#219871965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185239949-A-C

219872055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185239872-C-T

219873245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185238808-T-A

219873357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185238692-A-G

219874947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185237029-T-C

219875233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185236796-C-T

219875388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185236685-C-T

219875573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185236301-C-G

219875713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185236180-C-T

219875730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185236163-T-A

219875833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185236065-A-G

219876058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185234948-T-G

219876140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185234865-G-A

219876271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185234766-C-T

219876565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185234497-A-T

219877133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185234050-T-G

219877162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185234021-A-G

219877652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185233549-A-G

219877718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185233482-G-A

219877718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185233482-G-C

219877845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185233364-A-G

219877922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185233213-A-T

219877967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185233047-T-C

219877978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185233037-A-T

219878071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185232912-A-G

219878184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185232790-T-C

219878299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185232679-G-A

http://identifiers.org/hco/1/GRCh38#219878326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185232654-C-A

219878383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185232610-A-G

219878389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185232604-T-C

http://identifiers.org/hco/1/GRCh38#219878463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185232535-C-A

219878463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185232535-C-T

219878825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185232191-G-A

219879124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185231901-A-T

219879986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185231318-A-G

219880074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185231232-A-G

219880094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185231212-C-G

219880296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185231041-G-C

219880346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185230992-C-G

219880394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185230946-C-T

219880472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185230879-T-C

219881944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185226411-C-T

219882066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185226292-T-C

http://identifiers.org/hco/1/GRCh38#219882085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185226273-C-A

219882085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185226273-C-T

http://identifiers.org/hco/1/GRCh38#219882097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185226261-C-A

219882162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185226206-G-T

219882920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185225699-A-G

219882963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185225659-G-A

219897435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185216752-A-G

219897514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185216679-A-T

219897531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185216666-T-C

219897998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185216238-A-T

219897999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185216237-T-C

219898093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185216142-G-A

219898180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185216057-A-T

219898362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185215874-T-A

219898362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185215874-T-C

219898403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185215822-T-C

219898418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185215800-C-T

219898477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185215741-G-C

219898501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185215731-G-A

219898507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185215725-A-G

219898541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185215701-T-C

219898560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185215693-G-C

219898563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185215690-T-A

219898588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185215669-G-A

219898588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185215669-G-C

219898608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185215649-C-G

http://identifiers.org/hco/1/GRCh38#219901208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185212766-C-A

219902715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185209364-G-A

http://identifiers.org/hco/1/GRCh38#219903139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185208881-C-A

219903139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185208881-C-T

219903175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185208845-T-A

219903186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185208830-T-G

http://identifiers.org/hco/1/GRCh38#219903214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185208804-C-A

219903214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185208804-C-T

http://identifiers.org/hco/1/GRCh38#219903221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185208797-C-A

219903225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185208793-A-G

219903266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185208757-A-T

219903295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185208715-T-A

219903298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185208712-C-T

219903302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185208708-A-G

219903306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185208704-G-A

219905485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185203366-C-T

http://identifiers.org/hco/1/GRCh38#219905486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185203365-A-C

219905486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185203365-A-G

219905486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185203365-A-T

219905647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185203204-T-C

219905761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185203113-T-A

219905761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185203113-T-C

http://identifiers.org/hco/1/GRCh38#219905797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185203081-C-A

219905797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185203081-C-T

219905912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185202961-C-T

219906040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185202797-A-T

219906081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185202722-A-G

219906223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185202621-C-T

219906224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185202620-G-A

219906224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185202620-G-C

219906229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185202615-G-A

219906229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185202615-G-T

219906285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185202564-T-C

219906322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185202529-T-G

219907084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185202081-G-A

219907088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185202077-C-T

219907275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185201895-C-T

219907322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185201848-C-T

219907360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185201810-A-T

219910501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185200845-C-T

219910703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185200643-C-G

219910840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185200523-G-A

219910939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185200435-T-C

219911040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185200335-T-C

219912890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185199234-G-A

219912898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185199226-G-A

219913056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185199098-T-C

219913490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185198720-G-A

219913546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185198659-T-C

219913991-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185198258-A-T

219914021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185198203-G-A

219914122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185198098-A-G

http://identifiers.org/hco/1/GRCh38#219914222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185198009-C-A

219914531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185197715-G-A

219914531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185197715-G-T

219914533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185197713-T-A

219914533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185197713-T-C

219914856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185197459-C-G

219915069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185197177-T-A

219915123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185197086-A-G

219915141-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185197040-A-T

219915177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185196994-T-C

219915213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185196958-T-C

219915213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185196958-T-G

219915264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185196907-G-C

219915311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185196857-A-G

219915311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185196857-A-T

219915540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185196665-T-C

219915602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 185196618-G-A

219915602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 185196618-G-C

219915654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185196566-C-T

219915789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185196431-G-A

219915789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185196431-G-T

219915952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 185196268-T-C

http://identifiers.org/hco/1/GRCh38#219916025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185196175-C-A

219916025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185196175-C-G

219916025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185196175-C-T

219916059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185196144-T-A

219916059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185196144-T-C

http://identifiers.org/hco/1/GRCh38#219916064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185196139-C-A

219916064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185196139-C-T

219916113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185196096-A-G

219916113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185196096-A-T

219918123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185195245-C-T

http://identifiers.org/hco/1/GRCh38#219918174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#185195193-C-A

219918174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185195193-C-G

219918202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185195173-C-T

219918337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 185195039-C-T

219918371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 185195005-G-T

219918524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185194848-G-A

219918524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185194848-G-T

http://identifiers.org/hco/1/GRCh38#219918528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185194844-C-A

219918528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185194844-C-T

http://identifiers.org/hco/1/GRCh38#219918543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185194829-C-A

219918543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185194829-C-G

219918543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185194829-C-T

219918549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185194823-A-T

219918586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185194773-T-C

219918587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185194772-T-C

219918623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185194690-A-G

http://identifiers.org/hco/1/GRCh38#219918672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185194609-C-A

219918672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185194609-C-T

http://identifiers.org/hco/1/GRCh38#219918693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185194586-C-A

219918693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185194586-C-T

219918710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185194569-G-T

http://identifiers.org/hco/1/GRCh38#219918780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185194227-C-A

219918846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185194173-T-C

http://identifiers.org/hco/1/GRCh38#219918854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185194165-A-C

219918854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185194165-A-G

219918870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185194149-G-A

219918870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185194149-G-C

219918870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185194149-G-T

219918932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185194068-T-C

http://identifiers.org/hco/1/GRCh38#219918946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185194054-C-A

219918946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185194054-C-T

219918948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185194052-T-C

http://identifiers.org/hco/1/GRCh38#219918952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185194048-C-A

219918963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185194037-T-C

http://identifiers.org/hco/1/GRCh38#219919005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185194005-C-A

219919005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185194005-C-T

219919066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185193952-T-G

219919067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185193951-G-T

219926438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185190307-A-G

219926556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185190202-G-A

219926769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185188875-A-T

219926872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185188773-G-C

http://identifiers.org/hco/1/GRCh38#219927237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185188417-C-A

219927607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185188081-T-A

219927607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185188081-T-C

219927607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185188081-T-G

http://identifiers.org/hco/1/GRCh38#219927664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185188018-A-C

219927664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185188018-A-G

219927664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185188018-A-T

http://identifiers.org/hco/1/GRCh38#219927707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185187969-C-A

219927707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185187969-C-G

219927707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185187969-C-T

219927708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185187968-A-G

219927776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185187899-T-C

http://identifiers.org/hco/1/GRCh38#219927849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185187826-C-A

219927849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 185187826-C-G

219927849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 185187826-C-T

219927933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 185187760-G-A

219927941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 185187752-A-G

219927941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 185187752-A-T

http://identifiers.org/hco/1/GRCh38#219928001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#185187698-C-A

219928001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 185187698-C-G

219928001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 185187698-C-T

219928006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 185187693-G-A

219928006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 185187693-G-C

219928127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 185187572-G-A

219928127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 185187572-G-T

219928157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 185187542-G-A

219928234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 185187465-G-C

http://identifiers.org/hco/1/GRCh38#219928516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#185187218-C-A

219928516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185187218-C-T

http://identifiers.org/hco/1/GRCh38#219928560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185187185-C-A

219928560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185187185-C-T

219928572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185187171-G-A

219928572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185187171-G-C

219928572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185187171-G-T

http://identifiers.org/hco/1/GRCh38#219928701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185187059-C-A

219928701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185187059-C-T

http://identifiers.org/hco/1/GRCh38#219928737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#185187025-A-C

219928737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 185187025-A-G

219928797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185186970-G-T

219928852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185186900-G-C

219928871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185186881-C-T

219928973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 185186792-T-C

219929069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185186720-A-G

219929248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185186564-A-G

219929493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185186348-A-G

http://identifiers.org/hco/1/GRCh38#219930887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185184264-A-C

219931094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185184049-G-T

219931187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185183927-C-T

219931332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 185183783-G-A

219931386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185183733-G-T

219932348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185182785-G-T

http://identifiers.org/hco/1/GRCh38#219934590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185181505-C-A

219934590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185181505-C-T

219935308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185180386-T-G

219936166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185179165-C-T

219936192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185179140-C-G

219936358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185178977-G-A

219936504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185178640-C-T

219936523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185178621-C-G

219936523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185178621-C-T

219936567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185178575-A-G

219936636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185178455-G-A

219936663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185178432-C-G

219936692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185178403-C-T

219938847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185176601-C-T

219939818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185175102-A-G

219939963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185174969-T-A

219940167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185174807-G-A

219940224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185174746-T-A

219940334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185174635-C-T

http://identifiers.org/hco/1/GRCh38#219940367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185174601-C-A

219940379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185174589-G-A

219940792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185174296-T-A

219940815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185174273-G-A

http://identifiers.org/hco/1/GRCh38#219940912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185174174-C-A

219940912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185174174-C-G

219941019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185174066-G-A

219941256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185173856-A-G

219941289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185173837-A-G

219941322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185173803-G-T

219942209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185173266-G-A

219952257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185169424-C-T

219952380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185169315-A-G

219954095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185168413-T-G

219955516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185166990-A-G

219955753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185166775-A-G

219955784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185166757-T-C

http://identifiers.org/hco/1/GRCh38#219955826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185166719-A-C

219955850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185166668-T-C

219955933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185166562-G-A

219956018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185166476-T-A

219956018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185166476-T-C

219956094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185166437-G-A

219956102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185166429-T-C

219956883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185166045-C-T

http://identifiers.org/hco/1/GRCh38#219956884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185166044-C-A

219956922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185166020-T-G

219957612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185165456-T-C

219957977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185165102-A-G

219958063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185165025-A-G

219958173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185164929-T-A

219958173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185164929-T-C

219958252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185164867-G-A

219958259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185164860-C-T

219958587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 185164639-G-T

219958708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: missense variant
orthologous variants: 185164518-A-G

219958708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: missense variant
orthologous variants: 185164518-A-T

219958777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: missense variant
orthologous variants: 185164449-G-A

http://identifiers.org/hco/1/GRCh38#219958795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185164431-C-A

219958795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: missense variant
orthologous variants: 185164431-C-T

219958906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: missense variant
orthologous variants: 185164320-G-A

219958921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: missense variant
orthologous variants: 185164305-T-A

219958921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: missense variant
orthologous variants: 185164305-T-G

219958991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: missense variant
orthologous variants: 185164235-G-C

219958991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: missense variant
orthologous variants: 185164235-G-T

219959002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: missense variant
orthologous variants: 185164224-C-T

219959031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25355
most severe consequence: 5 prime UTR variant
orthologous variants: 185164205-C-T