http://identifiers.org/hco/14/GRCh38#104223602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112192066-C-A

104223602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: non coding transcript exon variant
orthologous variants: 112192066-C-T

104223690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: non coding transcript exon variant
orthologous variants: 112192135-A-G

104223737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: non coding transcript exon variant
orthologous variants: 112192159-C-T

104223760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: non coding transcript exon variant
orthologous variants: 112192182-A-G

104223790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: non coding transcript exon variant
orthologous variants: 112192213-C-T

104223861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112192279-C-G

104229907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112194845-C-T

104229996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112194908-A-G

104230011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112194920-C-T

http://identifiers.org/hco/14/GRCh38#104230026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112194936-A-C

104230026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112194936-A-T

104230068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112194974-C-T

104230116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112195036-G-A

104230257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112195170-C-T

104230584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112195648-C-T

104230636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112195697-G-A

http://identifiers.org/hco/14/GRCh38#104230684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112195737-C-A

104230684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112195737-C-T

104230720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112195759-G-T

104230834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112195866-G-A

104231049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112196050-G-T

104231089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112196128-C-T

104231119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112196227-C-T

104231136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112196258-T-C

104231158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112196285-G-A

104231404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112196507-C-G

104231435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112196537-G-A

104240413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112197603-A-G

104240426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112197616-C-T

104244122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112203187-A-G

http://identifiers.org/hco/14/GRCh38#104244158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112203243-C-A

104244158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112203243-C-G

104244158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112203243-C-T

104244280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112203354-T-C

104244284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112203358-T-C

104244337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112203410-C-T

http://identifiers.org/hco/14/GRCh38#104244376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112203448-C-A

104244378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112203450-T-C

104244409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112203479-G-A

104244409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112203479-G-C

104244409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112203479-G-T

104244441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112203509-C-G

104244441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112203509-C-T

104244517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112203549-G-A

http://identifiers.org/hco/14/GRCh38#104244907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112203933-C-A

104244926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112203952-T-A

http://identifiers.org/hco/14/GRCh38#104245172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112204100-C-A

104245590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112204496-C-G

104246884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112204532-G-A

http://identifiers.org/hco/14/GRCh38#104247035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112204688-A-C

104247041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112204694-C-G

104247065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112204716-C-T

104247090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112204741-G-A

104247090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112204741-G-T

104247203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112204818-G-T

104247428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112205033-C-T

104247480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112205099-G-T

104247563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112205176-C-T

http://identifiers.org/hco/14/GRCh38#104247572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112205188-C-A

104247572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112205188-C-T

104247843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112205449-G-A

104247843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112205449-G-T

104248107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112205736-C-T

104248228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112205851-G-C

104248425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112206045-G-A

104248425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112206045-G-C

104248618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112206233-G-A

104248645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112206259-G-C

104248695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112206291-A-T

104248698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112206294-C-T

104248709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112206305-A-G

http://identifiers.org/hco/14/GRCh38#104248774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112206373-C-A

104248774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112206373-C-T

104248802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112206401-G-A

104248802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112206401-G-T

104248895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112206504-C-T

104249007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112206621-C-T

104249097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112206677-A-G

104249414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112206808-G-A

104249414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112206808-G-T

104249617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112207008-C-T

104249893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112207217-G-A

104249956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112207253-A-G

104250006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112207293-G-A

104250361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112207536-A-G

104250368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112207546-G-T

104250417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112207594-T-C

104250436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112207607-C-G

104250490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112207635-A-G

104250532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112207666-G-A

104250532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112207666-G-C

104250545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112207679-G-A

104250545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112207679-G-C

104250624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112207745-G-C

104252124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112207833-A-T

http://identifiers.org/hco/14/GRCh38#104252157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112207860-C-A

104252205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112207907-C-T

104252286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112207972-G-C

104252460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112208164-C-T

104252575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112208280-C-T

104252588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112208296-G-A

104252597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112208305-G-A

104253051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112208713-G-A

104253118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112208792-A-T

104253233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112208923-G-A

104253248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112208938-C-T

104253287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112208989-G-T

104253538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112209162-C-G

http://identifiers.org/hco/14/GRCh38#104253599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112209213-C-A

104253599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112209213-C-T

104254026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112209677-A-G

http://identifiers.org/hco/14/GRCh38#104254035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112209686-A-C

104254114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112209748-G-A

104254114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112209748-G-T

http://identifiers.org/hco/14/GRCh38#104254257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112209887-C-A

104254257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112209887-C-T

104254462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112210095-A-G

104254525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112210167-G-A

104254556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112210211-G-A

104254589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112210245-C-T

104254832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112210533-G-C

104254923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112210622-A-G

104255111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112210773-T-C

104262260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214510-A-G

http://identifiers.org/hco/14/GRCh38#104262311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112214549-C-A

104262610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214846-G-A

104262645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214881-C-T

104262678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214921-G-A

104262776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112215017-C-T

104263176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112215523-G-C

104263245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112215590-C-T

104263259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112215607-T-G

104263365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112215717-C-G

104263509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112215846-C-T

104263574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112215910-G-A

104263713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112216051-C-T

104263826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112216164-G-A

104263934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112216244-G-C

104264057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112216369-A-G

104264242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112216587-A-T

http://identifiers.org/hco/14/GRCh38#104264379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112216716-A-C

104264407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112216741-G-A

104264566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112216913-C-T

http://identifiers.org/hco/14/GRCh38#104264860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112217104-C-A

104264860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112217104-C-T

104264953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112217181-C-T

104264973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112217196-G-A

104264994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112217217-C-T

104266704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112218861-G-A

104266906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112218993-G-A

http://identifiers.org/hco/14/GRCh38#104266909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112218996-C-A

104266909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112218996-C-T

104266912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112218999-A-G

104266913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112219000-C-T

http://identifiers.org/hco/14/GRCh38#104266977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112219061-C-A

104267046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112219143-G-A

104267130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112219255-G-A

104267338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112219550-C-T

104267339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112219551-G-A

104267450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112219639-C-G

104267546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112219705-C-T

104267833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112219986-C-G

104268003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112220166-C-T

104268102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112220255-G-A

104275835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

104275843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/14/GRCh38#104278766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112229720-C-A

104278766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112229720-C-T

104278988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112229939-A-G

104279128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112230069-G-A

104279128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112230069-G-T

104279190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112230114-G-A

104279190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112230114-G-C

104279196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112230120-G-A

104279196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112230120-G-C

http://identifiers.org/hco/14/GRCh38#104279567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112230471-C-A

http://identifiers.org/hco/14/GRCh38#104279706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112230551-C-A

104279799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112230643-G-A

http://identifiers.org/hco/14/GRCh38#104280013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112230871-A-C

104280032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112230891-C-G

104282716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112231898-A-G

104282736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112231910-C-T

104282976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112232112-G-A

104282988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112232121-C-T

104283277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112232415-G-A

104283316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112232442-A-G

104283316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112232442-A-T

104283415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112232552-C-T

104283597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112232733-C-G

104283597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112232733-C-T

104283644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112232772-C-T

104283670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112232811-A-G

104283750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112232890-T-C

104283787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112232926-G-A

104283955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112233095-G-A

104283955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112233095-G-T

http://identifiers.org/hco/14/GRCh38#104283979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112233119-C-A

104283979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112233119-C-T

104283993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112233133-G-T

http://identifiers.org/hco/14/GRCh38#104284063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112233209-C-A

104284082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112233238-C-T

104284317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112233414-G-A

104284403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112233502-G-C

104284457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112233548-C-T

http://identifiers.org/hco/14/GRCh38#104284483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112233574-A-C

104284518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112233639-G-A

104285471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112235747-C-T

http://identifiers.org/hco/14/GRCh38#104285574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112235843-C-A

104285648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20358
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112235915-G-A