97928546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106877652-T-C

97928557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106877663-T-A

97928628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106877729-A-G

http://identifiers.org/hco/14/GRCh38#97928735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106877825-C-A

97929005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106878087-G-T

97929028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106878110-G-A

97929099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106878167-A-G

97929137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106878205-T-C

97929208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106878275-G-A

http://identifiers.org/hco/14/GRCh38#97929236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106878303-C-A

97929485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106878479-T-C

97929580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106878572-G-A

97929580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106878572-G-T

97929670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106878647-C-T

http://identifiers.org/hco/14/GRCh38#97929746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106878706-C-A

97929838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106878797-C-T

http://identifiers.org/hco/14/GRCh38#97930108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106879036-A-C

97930295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106879216-T-C

97930296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106879217-G-T

97930356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106879271-C-T

97930407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106879320-C-T

http://identifiers.org/hco/14/GRCh38#97930476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106879383-C-A

97930476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106879383-C-G

97930476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106879383-C-T

http://identifiers.org/hco/14/GRCh38#97930538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106879439-C-A

97930699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106879600-T-C

97930950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106879978-G-C

97931227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106880255-G-T

97933529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106882467-T-C

97933529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106882467-T-G

http://identifiers.org/hco/14/GRCh38#97933536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106882474-C-A

97933550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106882488-A-G

97933559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106882497-G-T

97933570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106882508-C-T

97933583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106882521-A-G

97933660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106882604-T-C

97933663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106882607-T-C

97933675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106882625-C-T

97933833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106882777-T-C

97933840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106882784-G-T

97933969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106882891-G-T

http://identifiers.org/hco/14/GRCh38#97934094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106883016-C-A

97934126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106883048-G-A

97934605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106883403-A-G

97934682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106883463-A-G

97934851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106883555-G-T

97934860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106883564-G-T

97934926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106883634-G-T

97935022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106883716-C-T

97935290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106883924-G-T

97935412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106884011-C-T

97935575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106884040-C-G

97935575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106884040-C-T

97935821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106884522-A-G

http://identifiers.org/hco/14/GRCh38#97936196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106884848-C-A

97936196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106884848-C-G

97936196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106884848-C-T

http://identifiers.org/hco/14/GRCh38#97936204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106884856-A-C

97936204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106884856-A-T

97936302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106884933-G-T

97936309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106884940-T-C

97936371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106884992-C-T

97936700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106885323-T-A

97936725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106885347-G-A

97936757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106885380-T-C

http://identifiers.org/hco/14/GRCh38#97936777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106885400-C-A

97936816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106885435-C-T

97938053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106886336-T-C

http://identifiers.org/hco/14/GRCh38#97938122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106886411-C-A

97938170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106886460-G-A

97938170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106886460-G-C

97938220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106886501-A-G

97938229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106886510-G-A

97938231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106886512-C-T

97938297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106886566-G-A

97938470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106886711-G-T

97938535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106886776-T-C

97938634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106886908-T-C

97938844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106887120-G-T

97939077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106887299-A-G

97939103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106887327-G-T

97939109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106887333-A-G

97939174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106887405-C-T

97939188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106887417-C-T

97939194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106887423-C-T

97939226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106887455-G-A

97939226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106887455-G-T

97939298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106887524-C-T

97939568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106887728-G-A

97939568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106887728-G-T

http://identifiers.org/hco/14/GRCh38#97939781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106887929-A-C

97940206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106888336-T-C

97940232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106888356-A-G

97940733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106888808-G-T

97940779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106888849-T-C

97940883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106888956-A-G

97941004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106889092-T-C

97941051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106889150-G-T

97941163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106889250-A-G

97941272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106889341-A-G

97941433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106889518-G-C

97941542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106889627-T-C

97941549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106889634-A-G

http://identifiers.org/hco/14/GRCh38#97941574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106889659-C-A

97941708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106889784-A-G

97941928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106889982-G-A

http://identifiers.org/hco/14/GRCh38#97942069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106890119-C-A

97942128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106890171-C-T

97942708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106890875-C-T

97942727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106890910-T-G

97942829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106891328-T-G

97943040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106891540-A-T

97943134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106891644-G-A

97943134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106891644-G-T

97943159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106891669-C-T

http://identifiers.org/hco/14/GRCh38#97943163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106891673-C-A

97943163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106891673-C-T

97943165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106891698-C-T

97943412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106892113-G-T

97943483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106892185-G-T

97943536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106892238-A-G

97943568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106892272-C-T

97943845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106892777-G-A

97943845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106892777-G-T

97943862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106892794-C-T

97943991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106892922-C-G

97944084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106893031-A-T

97944185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106893125-G-A

97944302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106893216-A-G

97944363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106893264-T-C

97944809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106893603-G-A

97944816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106893608-C-T

97944956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106893747-A-G

97945126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106893897-T-C

97945281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106894037-G-A

97945281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106894037-G-T

97945337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106894106-A-G

http://identifiers.org/hco/14/GRCh38#97945887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106894677-C-A

97945887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106894677-C-G

97946337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106895118-T-G

http://identifiers.org/hco/14/GRCh38#97946379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106895161-A-C

97946389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106895171-G-T

97946579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106895349-C-T

97946587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106895356-C-T

http://identifiers.org/hco/14/GRCh38#97947001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106895801-C-A

97947083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106895882-T-A

97947274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106896030-A-G

97947618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106896342-C-T

97947982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106897071-G-A

97948065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106897178-C-T

97948077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106897190-G-A

97948077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106897190-G-T

97948088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106897201-G-A

97948089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106897202-A-G

97948144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106897272-G-A

97948144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106897272-G-C

http://identifiers.org/hco/14/GRCh38#97948214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106897340-C-A

97948214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106897340-C-T

97948227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106897353-G-T

http://identifiers.org/hco/14/GRCh38#97948402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106897479-C-A

http://identifiers.org/hco/14/GRCh38#97948448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106897524-C-A

97948530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106897588-C-T

97948536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106897594-C-T

97948690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106897747-C-T

97948796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106897855-A-G

http://identifiers.org/hco/14/GRCh38#97948895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106897940-C-A

97949416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106898515-C-T

97949514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106898621-A-G

http://identifiers.org/hco/14/GRCh38#97949631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106898703-C-A

97949631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106898703-C-G

97949636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106898708-T-G

97949639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106898711-A-G

97951198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106900793-G-A

97951198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106900793-G-T

97951359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106900923-A-G

97951407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106900974-T-A

97951407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106900974-T-G

97951422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106900989-A-G

97951425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106900992-G-T

97951426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106900993-T-C

97951431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106901001-T-G

97951497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106901067-C-T

97951521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106901088-C-T

97951857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106901254-T-C

97951881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106901272-A-G

97952082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106901452-G-A

http://identifiers.org/hco/14/GRCh38#97952110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106901480-A-C

97952165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106901532-A-G

97952216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106901700-G-A

97952218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106901702-G-A

http://identifiers.org/hco/14/GRCh38#97952328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106901874-A-C

97952402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106901941-G-A

97952455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106901995-G-A

97952456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106901996-C-T

97952463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106902003-G-A

97952739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106902276-C-T

97952762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106902299-A-G

97953201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106902649-T-C

97953289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106902722-G-T

97953290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106902723-A-G

http://identifiers.org/hco/14/GRCh38#97953296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106902728-A-C

97953349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106902777-T-A

97953368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106902798-T-C

97954255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106902918-G-T

http://identifiers.org/hco/14/GRCh38#97954256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106902919-C-A

97954256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106902919-C-T

97954296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106902962-A-T

http://identifiers.org/hco/14/GRCh38#97954420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106903076-C-A

97954427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106903083-A-G

97954443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106903099-C-T

97954455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106903110-G-A

97954460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106903115-C-T

97954836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106903374-C-T

97954890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106903711-G-A

97954898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106903719-T-C

97954899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106903720-A-G

97954941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106903761-A-G

97955256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106904059-A-G

97955325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106904130-A-G

97955495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106904298-G-A

97955684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106904507-G-A

http://identifiers.org/hco/14/GRCh38#97955710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106904536-A-C

97955710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106904536-A-G

97955734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106904581-A-T

97955753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106904616-A-T

http://identifiers.org/hco/14/GRCh38#97955976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106904862-A-C

97956251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106905114-C-T

97956661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106905368-G-T

97956714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106905415-T-C

97956823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106905507-G-A

97956949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106905621-G-A

97957025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106905728-T-C

97957325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106906021-A-T

97957340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106906036-C-T

http://identifiers.org/hco/14/GRCh38#97957675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106906349-A-C

97957683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106906357-T-C

97957715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106906389-T-C

97957753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106906429-A-G

97957781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106906456-T-C

http://identifiers.org/hco/14/GRCh38#97957800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106906475-C-A

97959068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106907971-A-G

97959083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106907986-C-T

97959229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106908126-G-T

http://identifiers.org/hco/14/GRCh38#97959298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106908191-C-A

http://identifiers.org/hco/14/GRCh38#97959459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106908348-C-A

97959459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106908348-C-T

97959543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106908430-G-A

97959543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106908430-G-T

97959596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106908484-A-G

97959600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106908488-T-C

97959637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106908512-A-G

97959684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106908556-T-C

97959750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106908615-A-G

97963866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106909327-G-T

97963924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106909385-A-T

97964328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106909731-A-T

97964409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106909814-T-A

http://identifiers.org/hco/14/GRCh38#97964508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106909913-C-A

97964508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106909913-C-T

http://identifiers.org/hco/14/GRCh38#97964691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106910090-C-A

97964691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106910090-C-T

97964732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106910155-C-G

97964762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106910184-C-T

http://identifiers.org/hco/14/GRCh38#97964919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106910342-C-A

97964919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106910342-C-G

97964919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106910342-C-T

97965229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106910627-G-A

97965395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106910778-T-A

97965507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106910873-T-A

97965512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106910878-G-A

97965525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106910889-T-C

97965630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106910989-A-G

http://identifiers.org/hco/14/GRCh38#97965881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106911234-C-A

97965998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106911349-G-A

97966195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106911530-G-A

97966281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106911612-G-A

97966319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106911651-T-A

http://identifiers.org/hco/14/GRCh38#97966330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106911662-A-C

97966406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106911738-G-A

97966406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106911738-G-C

97966406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106911738-G-T

97966561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106911898-T-C

97966569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106911901-G-T

97966793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106912087-G-T

97966865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106912147-G-A

97966917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106912195-C-T

97969059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106913669-G-A

97969059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106913669-G-C

97969059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106913669-G-T

97969187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106913803-T-C

97969198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106913813-A-G

97969239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106913862-C-T

97969358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106913962-G-A

http://identifiers.org/hco/14/GRCh38#97969366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106913970-C-A

97969366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106913970-C-T

97969407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106914007-C-T

97969445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106914044-G-A

97969445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106914044-G-C

97969510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106914105-T-A

97969510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106914105-T-G

97969518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106914113-T-C

97969570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106914163-T-A

97969570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106914163-T-C

97969594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106914187-A-G

97969630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106914208-A-G

97969644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106914221-G-T

97969662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106914238-T-C

http://identifiers.org/hco/14/GRCh38#97969682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106914258-A-C

97969695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106914271-T-A

97969695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106914271-T-C

97969823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106914428-A-G

97969836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106914441-G-A

97969836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106914441-G-C

97969917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106914516-T-C

97969934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106914533-G-A

97969968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106914562-A-G

http://identifiers.org/hco/14/GRCh38#97970062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106914658-C-A

97970141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106914736-G-A

97970487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106915560-C-G

97973287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106917709-T-G

97973765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106917417-C-T

97973939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106917599-C-T

97973942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106917602-G-A

97974061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106917709-T-C

http://identifiers.org/hco/14/GRCh38#97974148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106917795-C-A

97974148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106917795-C-T

97974679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106918365-A-G

97974804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106918495-T-C

97974804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106918495-T-G

http://identifiers.org/hco/14/GRCh38#97974821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106918512-C-A

97974857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106918543-T-C

http://identifiers.org/hco/14/GRCh38#97974969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106918653-C-A

97975188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106918873-C-T

97975630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106919335-A-G

97975958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106920197-G-A

97976042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106920275-C-T

97976816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106920827-C-G

97976816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106920827-C-T

97976949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106920944-T-C

97977080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106921066-A-T

97977116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106921102-G-A

97977157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106921139-C-T

97977294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106921295-A-T

97977336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106921340-G-C

http://identifiers.org/hco/14/GRCh38#97977419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106921531-C-A

http://identifiers.org/hco/14/GRCh38#97977471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106921630-C-A

97977471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106921630-C-T

97977523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106921685-T-C

http://identifiers.org/hco/14/GRCh38#97977552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106921714-A-C

97977552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106921714-A-T

97977622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106921784-A-T

97977637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106921799-C-T

97977668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106921821-G-T

97977698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106921851-G-A

97977814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106921919-C-T

http://identifiers.org/hco/14/GRCh38#97977898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106921996-A-C

97977898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106921996-A-G

97977898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106921996-A-T

97977948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106922033-G-C

97977948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106922033-G-T

http://identifiers.org/hco/14/GRCh38#97977951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106922036-C-A

97977951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106922036-C-T

http://identifiers.org/hco/14/GRCh38#97977954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#106922039-C-A

97977958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106922043-T-A

97977958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106922043-T-C

97978029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: non coding transcript exon variant
orthologous variants: 106922109-T-C

97978032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: non coding transcript exon variant
orthologous variants: 106922112-T-A

97978032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: non coding transcript exon variant
orthologous variants: 106922112-T-C

97978032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20111
most severe consequence: non coding transcript exon variant
orthologous variants: 106922112-T-G