2631985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 5 prime UTR variant
orthologous variants: 140634751-A-G

2631985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 5 prime UTR variant
orthologous variants: 140634751-A-T

2632001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 5 prime UTR variant
orthologous variants: 140634735-G-A

2632001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 5 prime UTR variant
orthologous variants: 140634735-G-C

2632001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 5 prime UTR variant
orthologous variants: 140634735-G-T

2632536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140634301-G-C

2632542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140634295-C-G

2632633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140634213-G-A

2633513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140633453-C-G

2633673-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140633316-T-A

http://identifiers.org/hco/7/GRCh38#2633674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140633315-C-A

2633718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, undefined
orthologous variants: 140633290-C-G

http://identifiers.org/hco/7/GRCh38#2633735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140633276-C-A

2634225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140632872-C-T

2634326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140632780-G-A

2634353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140632755-G-A

2634938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140632186-G-C

2635126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140631961-A-G

2635170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140631918-G-A

2635274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140631820-G-T

2635293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140631799-C-T

2635450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140631702-A-G

2635552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140631583-C-T

http://identifiers.org/hco/7/GRCh38#2635557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140631578-C-A

2635557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140631578-C-T

2635661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140631494-T-C

2635775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140631381-A-G

2635781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140631375-G-A

2636030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140630953-C-T

2637318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140628299-C-T

2637327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140628290-G-A

2637333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140628284-T-C

2637580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, undefined
orthologous variants: 140628085-C-T

2637690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, undefined
orthologous variants: 140627981-G-A

2638776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, undefined
orthologous variants: 140627426-A-G

2638784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, undefined
orthologous variants: 140627416-G-A

2638967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140627180-C-T

2639163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140627010-C-T

2641465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, undefined
orthologous variants: 140626038-A-G

2641526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, undefined
orthologous variants: 140625983-G-A

2641526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, undefined
orthologous variants: 140625983-G-C

2641719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, undefined
orthologous variants: 140625811-C-T

2641803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, undefined
orthologous variants: 140625727-G-A

2641809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, undefined
orthologous variants: 140625721-C-T

2644205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140623708-G-A

2644275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140623658-C-T

2644300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140623633-C-T

http://identifiers.org/hco/7/GRCh38#2644355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140623575-A-C

2644437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140623471-T-C

2644636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140623333-C-G

2644691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140623276-C-T

2644704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140623263-G-T

2644780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140623125-C-T

2646872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense variant
orthologous variants: 140621800-C-T

http://identifiers.org/hco/7/GRCh38#2646910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140621762-C-A

2646910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: synonymous variant
orthologous variants: 140621762-C-T

2646967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense_variant, undefined
orthologous variants: 140621705-G-C

2646967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense_variant, undefined
orthologous variants: 140621705-G-T

2647004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense_variant, undefined
orthologous variants: 140621668-T-C

2647032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140621577-G-A

2647046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140621542-G-A

2647075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, undefined
orthologous variants: 140621463-G-A

2647075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, undefined
orthologous variants: 140621463-G-T

2647149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense variant
orthologous variants: 140621371-A-G

2647149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense variant
orthologous variants: 140621371-A-T

2647189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense variant
orthologous variants: 140621331-G-A

2647200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense variant
orthologous variants: 140621320-G-A

2647200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense variant
orthologous variants: 140621320-G-T

2647286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140621243-T-A

2647286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140621243-T-C

2647433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense variant
orthologous variants: 140621140-G-A

2647470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense variant
orthologous variants: 140621103-C-T

2647496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense variant
orthologous variants: 140621077-C-T

2647540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense variant
orthologous variants: 140621033-G-T

http://identifiers.org/hco/7/GRCh38#2647557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140621016-C-A

2647557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense variant
orthologous variants: 140621016-C-T

http://identifiers.org/hco/7/GRCh38#2647646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140620927-C-A

2647646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 140620927-C-G

2647646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 140620927-C-T

2647667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140620894-C-G

2647682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140620880-A-G

2647770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 140620828-A-G

2648103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140620452-G-A

2648103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140620452-G-T

http://identifiers.org/hco/7/GRCh38#2648112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140620443-C-A

2648112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140620443-C-G

2648112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140620443-C-T

http://identifiers.org/hco/7/GRCh38#2648155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140620394-A-C

2648155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140620394-A-G

2648176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140620380-G-A

2648176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140620380-G-T

2648259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140620303-A-G

http://identifiers.org/hco/7/GRCh38#2648295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140620280-C-A

2648295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140620280-C-T

http://identifiers.org/hco/7/GRCh38#2648331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140620258-C-A

2648331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140620258-C-T

2648479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140620182-T-G

http://identifiers.org/hco/7/GRCh38#2648522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140620147-C-A

2648522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140620147-C-T

2648569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140620105-A-G

2648590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140620083-G-A

2648590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140620083-G-C

2648590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140620083-G-T

2648608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140620065-T-C

2648608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140620065-T-G

2648617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140620055-T-A

http://identifiers.org/hco/7/GRCh38#2648627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140620045-C-A

2648655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140620018-G-A

2648655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140620018-G-T

2648766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619923-T-G

2648775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619918-A-G

2648867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619847-G-T

2648891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619844-G-A

2648911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619824-G-A

2649082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619770-A-G

2649380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619572-G-C

2649402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619550-G-A

2649420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619536-G-A

2649420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619536-G-T

2649454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619503-T-C

2649454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619503-T-G

2649464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619494-G-A

2649481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619473-G-C

2649481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619473-G-T

2649517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619431-A-G

2649517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619431-A-T

2649657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619299-T-C

http://identifiers.org/hco/7/GRCh38#2649666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140619290-C-A

2649666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619290-C-G

2649666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619290-C-T

2649682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619274-G-A

2649682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619274-G-C

2649682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619274-G-T

http://identifiers.org/hco/7/GRCh38#2649722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140619244-C-A

2649722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619244-C-G

2649722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140619244-C-T

2650004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140619002-C-G

2650004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140619002-C-T

http://identifiers.org/hco/7/GRCh38#2650037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140618984-C-A

2650037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140618984-C-G

2650037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140618984-C-T

2650048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140618973-G-A

2650048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140618973-G-C

http://identifiers.org/hco/7/GRCh38#2650076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140618945-C-A

2650076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140618945-C-T

2650083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140618938-G-T

2650151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140618872-C-T

2652058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140618132-G-T

2652083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140618106-G-A

2652083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140618106-G-C

2652083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140618106-G-T

2652100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140618082-A-T

2652105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140618077-T-A

2652105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140618077-T-C

2652213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense variant
orthologous variants: 140617970-T-A

2652219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense variant
orthologous variants: 140617964-C-G

2652219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense variant
orthologous variants: 140617964-C-T

2652262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140617925-G-A

2652262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140617925-G-T

2652297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140617890-G-A

2652297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140617890-G-T

2652300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140617887-T-C

2652302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140617885-T-C

2652309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140617878-G-A

2652309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140617878-G-T

2652467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140617751-T-C

2652540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140617684-C-G

2652597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140617626-G-A

2652601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140617622-C-T

2652728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140617501-G-T

2652776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140617447-T-C

2652790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140617432-G-A

2652790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140617432-G-T

2652846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140617405-T-G

http://identifiers.org/hco/7/GRCh38#2652883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140617363-C-A

2652883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140617363-C-T

http://identifiers.org/hco/7/GRCh38#2652907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140617349-C-A

2652924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140617332-T-C

2655989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140615641-T-G

2656003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140615635-A-G

2656125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140615527-G-A

2656125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140615527-G-T

2656321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140615348-G-A

2656321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140615348-G-C

2656321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140615348-G-T

2656378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140615287-A-G

http://identifiers.org/hco/7/GRCh38#2656383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140615282-A-C

2656636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140615104-G-C

2656653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140615087-T-G

http://identifiers.org/hco/7/GRCh38#2656660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140615080-C-A

2656660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140615080-C-T

http://identifiers.org/hco/7/GRCh38#2656662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140615078-C-A

2656662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140615078-C-G

2656662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140615078-C-T

2656918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140614870-G-A

2656989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140614816-G-C

2657386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140613996-A-G

2657386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140613996-A-T

2657394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140613987-G-T

2657397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140613984-G-A

2657413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140613968-G-A

2658099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140613226-C-T

2658119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140613198-G-A

2658148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140613169-T-A

2658148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140613169-T-C

2658160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140613157-T-G

2658169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140613145-G-A

2658169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140613145-G-T

2658170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140613144-G-A

http://identifiers.org/hco/7/GRCh38#2658206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140613117-A-C

2658206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140613117-A-G

2658206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140613117-A-T

http://identifiers.org/hco/7/GRCh38#2658219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140613106-C-A

2658219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140613106-C-T

2658239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140613093-T-C

http://identifiers.org/hco/7/GRCh38#2658275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140613059-C-A

2658275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140613059-C-T

http://identifiers.org/hco/7/GRCh38#2658279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140613055-C-A

2658305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 140613029-G-T

2658317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140613017-G-A

2658317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140613017-G-T

2658544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140612768-A-G

http://identifiers.org/hco/7/GRCh38#2658872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140612344-C-A

2658872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140612344-C-T

http://identifiers.org/hco/7/GRCh38#2658881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140612337-C-A

2658881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140612337-C-T

http://identifiers.org/hco/7/GRCh38#2658902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140612316-C-A

2658902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140612316-C-T

2658917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140612303-G-C

http://identifiers.org/hco/7/GRCh38#2659051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140612170-C-A

http://identifiers.org/hco/7/GRCh38#2659077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140612143-C-A

2659077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140612143-C-G

2659097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140612123-G-T

2659104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140612116-G-A

2659104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140612116-G-T

2659630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140611240-T-G

2659743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140611124-G-C

http://identifiers.org/hco/7/GRCh38#2659872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140611011-C-A

2659872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140611011-C-T

2660112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140610770-G-A

2660112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140610770-G-T

2660252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140610694-C-T

http://identifiers.org/hco/7/GRCh38#2660453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#140610542-C-A

2660453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, undefined
orthologous variants: 140610542-C-T

2660514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140610492-G-A

2660545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140610462-G-A

2660545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140610462-G-C

2660664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140610337-G-A

2660664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140610337-G-T

2660787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140610220-G-A

2660833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, undefined
orthologous variants: 140610173-G-A

2660833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, undefined
orthologous variants: 140610173-G-C

2660924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron_variant, undefined
orthologous variants: 140610049-C-T

2661568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140609391-G-C

2661624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140609334-C-T

2661658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: intron variant
orthologous variants: 140609297-C-T

2661743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140609206-G-A

2661743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140609206-G-T

2661748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140609200-C-T

2661762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140609184-C-G

2661822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140609129-G-A

2661822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140609129-G-T

2661839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140609111-G-A

2661839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140609111-G-T

http://identifiers.org/hco/7/GRCh38#2661877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140609077-C-A

2661877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140609077-C-G

2661877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140609077-C-T

http://identifiers.org/hco/7/GRCh38#2661933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140609019-C-A

2661933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140609019-C-G

2661933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140609019-C-T

http://identifiers.org/hco/7/GRCh38#2661956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140608985-C-A

2661956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140608985-C-T

2662059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140608879-T-A

2662059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140608879-T-C

2662059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140608879-T-G

2662298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140608646-G-A

2662298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140608646-G-T

http://identifiers.org/hco/7/GRCh38#2662440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140608511-C-A

2662440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140608511-C-T

2662517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140608430-T-C

http://identifiers.org/hco/7/GRCh38#2662608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140608343-C-A

http://identifiers.org/hco/7/GRCh38#2662699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140608244-C-A

2662699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140608244-C-T

2662700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140608243-A-G

http://identifiers.org/hco/7/GRCh38#2662708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140608235-C-A

2662708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140608235-C-T

http://identifiers.org/hco/7/GRCh38#2662712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140608231-C-A

2662712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140608231-C-T

2662969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 140608011-G-A

2663068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140607918-G-T

2663100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140607893-A-G

2663358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140607680-G-A

2663373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 140607665-T-A

2663373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 140607665-T-C

2663439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140607620-G-C

2663503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140607558-A-G

2663565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140607492-A-G

http://identifiers.org/hco/7/GRCh38#2663588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140607467-C-A

2663588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140607467-C-G

2663640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140607438-C-T

2663893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140607177-A-T

2663913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140607159-G-A

2663913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140607159-G-T

http://identifiers.org/hco/7/GRCh38#2664245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140606809-C-A

2664252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140606802-C-T

http://identifiers.org/hco/7/GRCh38#2664359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140606690-C-A

2664359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140606690-C-T

2664466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140606629-T-C

2664592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140606534-T-C

2664801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22222
most severe consequence: 3 prime UTR variant
orthologous variants: 140606331-A-G