112086441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45474366-G-A

112086441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45474366-G-C

112086441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 45474366-G-T

112086454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45474353-C-T

112086470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 45474337-G-A

112086531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45474276-G-A

112086531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45474276-G-T

112086584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45474241-C-T

http://identifiers.org/hco/3/GRCh38#112086611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45474217-C-A

112086611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45474217-C-T

http://identifiers.org/hco/3/GRCh38#112086645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45474185-C-A

112086645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45474185-C-G

112086645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45474185-C-T

http://identifiers.org/hco/3/GRCh38#112086648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45474182-C-A

112086648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45474182-C-T

http://identifiers.org/hco/3/GRCh38#112086923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45473941-C-A

112086927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45473937-C-T

112087026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45473817-A-T

112087071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45473769-C-T

http://identifiers.org/hco/3/GRCh38#112087329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45473571-C-A

112087335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45473564-C-G

112087598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45473330-T-C

112088196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45472752-G-A

112088774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45471443-C-G

112089570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45471007-G-T

112089598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45470982-T-C

112089615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45470965-G-A

112093006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45470036-A-G

112093052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45469995-T-C

112093125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45469928-T-G

112093237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45469448-A-G

112093237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45469448-A-T

112093278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45469404-T-G

112093288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45469397-G-A

112093452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45469231-C-T

112093560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45469133-A-G

http://identifiers.org/hco/3/GRCh38#112093579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45469114-C-A

112094835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45467994-C-G

http://identifiers.org/hco/3/GRCh38#112095144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45467747-A-C

112095197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45467695-G-C

112095230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45467663-C-T

http://identifiers.org/hco/3/GRCh38#112095499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45467417-C-A

112095599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45467306-A-G

112095970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45466324-G-T

112095999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45466302-G-A

112095999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45466302-G-C

112096051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45466267-A-G

http://identifiers.org/hco/3/GRCh38#112096653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45466117-A-C

112096653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45466117-A-T

112096760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45466024-G-C

112096909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45465891-A-G

112096989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45465813-A-T

112097103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45465676-T-C

112097179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45465269-T-G

112097200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45465248-T-G

http://identifiers.org/hco/3/GRCh38#112097201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45465247-C-A

http://identifiers.org/hco/3/GRCh38#112097376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45465170-C-A

http://identifiers.org/hco/3/GRCh38#112097646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45464922-C-A

112097722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45464845-T-G

112097770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45464797-C-T

http://identifiers.org/hco/3/GRCh38#112097787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45464776-C-A

112098081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45464673-A-G

112098289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45464473-C-T

112098319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45464444-T-C

112101753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45461911-A-T

112101896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45461720-T-A

112101896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45461720-T-G

112101910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45461706-G-A

112101913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45461703-G-A

112101913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45461703-G-T

112102051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45461556-A-G

112102064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45461542-T-A

112102430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45461299-A-T

112102638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45461143-A-T

112102818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45460813-A-T

112102879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45460752-T-C

http://identifiers.org/hco/3/GRCh38#112102902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45460729-C-A

112102902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45460729-C-T

112102904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45460727-T-C

112102976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45460655-C-G

112102979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45460652-A-G

112102982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45460649-T-C

112102996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45460635-T-A

112103814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45459868-G-A

112104060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45459627-G-A

http://identifiers.org/hco/3/GRCh38#112104150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45459543-A-C

112107332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45457152-A-G

112107469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45457017-A-G

112108279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45456028-T-C

112108300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45456013-G-A

112108314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45456000-T-G

112108495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45455824-C-T

112108527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45455793-G-A

112108558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45455759-G-C

112109122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45454053-C-T

112109181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45453996-T-A

112109181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45453996-T-C

112109244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45453945-T-C

112109244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45453945-T-G

112109436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45453514-G-A

112109436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45453514-G-T

112109472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45453480-T-C

112109475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45453477-T-C

112109477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45453475-T-C

http://identifiers.org/hco/3/GRCh38#112109568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45453387-C-A

112109568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45453387-C-G

112109568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45453387-C-T

112109617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45453338-A-G

112109660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45453292-A-T

http://identifiers.org/hco/3/GRCh38#112109671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45453281-C-A

112109671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45453281-C-T

112109733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45453219-A-G

http://identifiers.org/hco/3/GRCh38#112109817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45453148-C-A

112109817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45453148-C-G

112109824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45453140-T-A

112109843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45453121-G-A

112109843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45453121-G-T

112109858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45453107-G-T

112109919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45453043-G-C

112109936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45453026-G-A

112110478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45452855-T-C

112111369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45451510-G-A

112111369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45451510-G-T

http://identifiers.org/hco/3/GRCh38#112111471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45451423-C-A

112111481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45451413-G-T

112111552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45451342-A-G

112111594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45451288-G-T

http://identifiers.org/hco/3/GRCh38#112111653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45451229-C-A

112111715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45451161-T-C

112111904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45450988-C-T

112112017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45450884-A-T

112112109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45450790-T-A

112112109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45450790-T-C

112112294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45450585-A-G

112112294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45450585-A-T

http://identifiers.org/hco/3/GRCh38#112112538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45450309-C-A

112112538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45450309-C-T

112112548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45450299-G-A

112112559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45450288-A-G

112112567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45450280-G-A

http://identifiers.org/hco/3/GRCh38#112112601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45450257-C-A

112112601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45450257-C-G

112112668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45450193-G-A

http://identifiers.org/hco/3/GRCh38#112112793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45450104-A-C

112112793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45450104-A-G

112112807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45450092-T-C

112112840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45450059-T-A

112112840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45450059-T-G

112113235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45449703-G-T

112116298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45449453-C-T

112116353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45449393-T-C

112116613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45448700-A-G

112116647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45448666-A-G

112116664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45448650-T-A

112116696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45448623-G-A

http://identifiers.org/hco/3/GRCh38#112116790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45448564-C-A

112116790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45448564-C-G

112116790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45448564-C-T

112116799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45448555-A-G

112116806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45448538-G-A

112116851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45448496-G-A

112117063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45448401-T-C

112117115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45448346-A-G

112117158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45448296-G-C

112117158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45448296-G-T

http://identifiers.org/hco/3/GRCh38#112117189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45448265-C-A

112117189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45448265-C-G

112117189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45448265-C-T

http://identifiers.org/hco/3/GRCh38#112117205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45448249-C-A

112117205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45448249-C-G

112117205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45448249-C-T

112117316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45448149-A-G

112117452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45448005-T-C

112117455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45448002-G-C

112117490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45447968-G-T

112117739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45447701-T-C

112118142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45447277-A-G

112118793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45446356-G-A

112118793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45446356-G-T

112118992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45445895-G-A

112119060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45445833-A-G

112120498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45445390-G-A

http://identifiers.org/hco/3/GRCh38#112120718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45444674-C-A

http://identifiers.org/hco/3/GRCh38#112120773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45444611-C-A

http://identifiers.org/hco/3/GRCh38#112120791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45444594-A-C

112121372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45443012-A-G

112121376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45443008-G-C

112121376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45443008-G-T

112121382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45443002-T-G

112121468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45442530-A-G

112121616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45442390-A-G

http://identifiers.org/hco/3/GRCh38#112121663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45442339-C-A

http://identifiers.org/hco/3/GRCh38#112121664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45442338-C-A

112121672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45442330-A-G

http://identifiers.org/hco/3/GRCh38#112121779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45442227-C-A

112121780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45442226-A-G

112122095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45441854-C-G

112122385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45441558-G-A

112122446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45441498-T-C

112122450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45441494-T-C

112122499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45441446-T-C

112122499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45441446-T-G

112122562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45441385-A-G

112122616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45441366-C-T

112122800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45441205-G-A

112122816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45441189-A-G

http://identifiers.org/hco/3/GRCh38#112122974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45440964-C-A

112122974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45440964-C-T

112122975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45440963-A-T

112123041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45440896-T-A

112123041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45440896-T-C

http://identifiers.org/hco/3/GRCh38#112123244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45440701-C-A

112123244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45440701-C-T

112123293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45440652-G-T

http://identifiers.org/hco/3/GRCh38#112123320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45440630-A-C

112123320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45440630-A-G

112123341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45440613-G-A

112123341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45440613-G-C

112123341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45440613-G-T

112123359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45440595-G-C

112123359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45440595-G-T

112123375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45440580-G-C

112123380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45440575-A-G

112123439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45440515-T-C

http://identifiers.org/hco/3/GRCh38#112123492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45440462-A-C

112123492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 45440462-A-G

112123633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 45440324-G-A

112123662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 45440295-A-G

112123818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45440139-T-C

112123873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45440082-T-A

112123873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45440082-T-C

112123873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45440082-T-G

112123892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45440063-T-C

112123892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45440063-T-G

112123902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45440058-A-G

http://identifiers.org/hco/3/GRCh38#112124772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45439567-A-C

112124802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45439537-A-G

http://identifiers.org/hco/3/GRCh38#112124894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45439446-A-C

http://identifiers.org/hco/3/GRCh38#112125081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45439273-C-A

112125081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45439273-C-T

http://identifiers.org/hco/3/GRCh38#112125121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45439236-C-A

112125130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45439227-G-T

112125245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 45439188-A-T

112125283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45439150-T-C

112125306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45439127-G-T

112125350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45439091-G-A

112125350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45439091-G-T

112125557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45438927-T-C

112125567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45438920-T-A

112125772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45438741-C-G

http://identifiers.org/hco/3/GRCh38#112125808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45438704-A-C

112125868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45438658-T-C

112126007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45438535-T-C

112126545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45438088-G-A

112126647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45437856-G-T

112126695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45437763-T-G

112126696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45437762-T-G

112126705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45437753-G-A

112126827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45437475-A-G

112126827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45437475-A-T

112126862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45437421-G-A

112126914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45437370-G-A

112126914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45437370-G-T

112127021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 45437263-G-A

112127021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 45437263-G-T

112127081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45437202-A-G

112127161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45437132-A-G

112127171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45437122-T-G

112127184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45437109-A-G

112127184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45437109-A-T

112127284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45437030-T-C

http://identifiers.org/hco/3/GRCh38#112127366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45436954-A-C

112127366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45436954-A-G

112127763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45436621-T-C

http://identifiers.org/hco/3/GRCh38#112127885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45436499-C-A

112127894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45436491-G-T

112127898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45436487-G-A

112127898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45436487-G-T

112127921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45436464-C-T

112128040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 45436345-A-G

112128071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45436311-C-G

http://identifiers.org/hco/3/GRCh38#112128117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45436261-A-C

112128121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45436257-G-T

112128139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45436235-A-G

112128146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45436228-T-G

http://identifiers.org/hco/3/GRCh38#112128164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45436176-C-A

112128164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45436176-C-G

112128164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45436176-C-T

http://identifiers.org/hco/3/GRCh38#112128165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45436175-C-A

112128165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45436175-C-T

112128185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_variant, stop_lost, undefined
orthologous variants: 45436157-A-G

http://identifiers.org/hco/3/GRCh38#112128218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45436089-C-A

112128218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 45436089-C-G

112128218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 45436089-C-T

112128272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45435919-G-T

112128316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45435871-T-C

112128438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45435640-A-G

112128454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45435543-A-G

112128538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45435427-A-G

112128691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45435306-G-A

112128691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45435306-G-C

112128691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45435306-G-T

112128692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45435305-T-A

112128692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45435305-T-C

112128692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45435305-T-G

112128727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45435270-T-A

112128727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45435270-T-C

112128727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45435270-T-G

http://identifiers.org/hco/3/GRCh38#112128749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45435245-C-A

112128749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45435245-C-G

http://identifiers.org/hco/3/GRCh38#112128851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45435152-C-A

112128898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45435099-G-T

112129339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45434636-G-A

http://identifiers.org/hco/3/GRCh38#112129416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45434561-C-A

112129416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45434561-C-T

112129422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45434555-T-C

112129503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45434372-A-G

112129597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45434229-A-G

112129637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45434191-T-C

112129674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45434152-A-G

http://identifiers.org/hco/3/GRCh38#112129851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45433990-C-A

http://identifiers.org/hco/3/GRCh38#112129869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45433972-C-A

112129869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45433972-C-T

112129871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45433970-G-T

http://identifiers.org/hco/3/GRCh38#112130072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45433782-C-A

112130072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45433782-C-T

112130256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45433607-A-G

http://identifiers.org/hco/3/GRCh38#112130261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45433602-A-C

112130261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45433602-A-G

112130261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45433602-A-T

http://identifiers.org/hco/3/GRCh38#112130277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45433586-A-C

112130331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45433535-A-G

112130331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45433535-A-T

112130556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45433338-C-T

http://identifiers.org/hco/3/GRCh38#112130642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45433246-A-C

112130667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45433221-G-A

112130667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45433221-G-T

112130696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45433189-C-T

112130887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45433066-A-G

http://identifiers.org/hco/3/GRCh38#112130950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45433030-C-A

112130950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45433030-C-T

http://identifiers.org/hco/3/GRCh38#112131000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45432976-A-C

112131000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45432976-A-G

112131329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45432660-C-G

112131722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45432363-T-C

112132251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45431676-T-C

112132251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45431676-T-G

112132444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45431501-G-C

http://identifiers.org/hco/3/GRCh38#112132532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45431420-C-A

112132546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45431406-G-A

112132546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45431406-G-T

http://identifiers.org/hco/3/GRCh38#112132637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45431318-C-A

112132891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45431083-T-C

112132972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45431008-T-C

112132981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45431001-A-G

112133053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45430956-C-T

112133054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45430955-C-G

112133149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45430865-C-G

112133149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26255
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45430865-C-T