http://identifiers.org/hco/10/GRCh38#125896690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#133378743-C-A

125896690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, undefined
orthologous variants: 133378743-C-G

125896690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, undefined
orthologous variants: 133378743-C-T

125897264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133379920-T-C

125897395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133380052-C-T

125897441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133380098-A-T

125897513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133380171-T-A

125897513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133380171-T-C

125897780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133380471-C-G

125897791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133380482-G-C

125898271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133380860-G-A

125898271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133380860-G-T

125899221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133381633-T-C

125899329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133381729-G-C

http://identifiers.org/hco/10/GRCh38#125899558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133381979-C-A

125899694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133382084-C-G

125900312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133382678-T-C

125900319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133382687-C-T

125900320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133382688-G-A

125900320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133382688-G-T

125900338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133382707-G-T

125900556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133383026-G-A

125901090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, undefined
orthologous variants: 133383344-G-A

125901130-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, undefined
orthologous variants: 133383404-T-G

125901200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, undefined
orthologous variants: 133383473-T-C

125901298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, undefined
orthologous variants: 133383572-A-G

125901324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, undefined
orthologous variants: 133383578-C-G

125901350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, undefined
orthologous variants: 133383627-C-G

125901350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, undefined
orthologous variants: 133383627-C-T

125901358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, undefined
orthologous variants: 133383635-G-A

125901388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, undefined
orthologous variants: 133383666-T-C

125901481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133383715-G-T

125901529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133383760-C-G

125901529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133383760-C-T

125901531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133383762-C-T

125901721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133383903-A-G

125901776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133383959-C-T

125902922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133384271-T-C

125902961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133384318-T-A

125903003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133384363-C-G

125903172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, undefined
orthologous variants: 133384516-G-A

125903379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, undefined
orthologous variants: 133384732-A-T

125903480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, undefined
orthologous variants: 133384824-C-G

125911805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133393853-C-T

125912068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133394095-T-C

125912129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, undefined
orthologous variants: 133394156-A-G

125912312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133394340-G-A

125912314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, undefined
orthologous variants: 133394342-G-A

125912354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133394382-C-T

125934498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133407581-G-A

125934713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133407782-G-C

125934713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133407782-G-T

125934876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133407923-C-T

125934956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133407993-C-T

125935094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133408163-A-G

125935214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133408254-G-C

125935317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133408361-G-T

125935510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133408547-G-T

125935836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133408860-A-G

125936224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133409200-C-T

125936478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133409413-T-A

125936478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133409413-T-C

125936480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133409415-C-T

125939569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133415023-A-T

125939621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133415077-G-A

125953401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133430098-G-A

125953423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133430120-G-A

125953440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133430160-A-T

125953777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133430419-C-T

125955931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133431454-C-G

125956051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133431566-A-G

125956219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133431741-T-A

125956219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133431741-T-C

125956219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133431741-T-G

125956225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133431747-T-A

125956225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133431747-T-C

125956225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133431747-T-G

125956345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133431856-A-G

125956350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133431861-A-G

125956384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133431896-C-T

125956407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133431907-T-C

125956462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133431964-A-G

125956483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133431985-C-G

125956527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133432027-T-C

125956727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133432219-T-C

125956763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133432255-G-A

125956763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133432255-G-T

125956781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133432273-T-C

125971600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133451209-G-A

125971600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133451209-G-T

125972959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133451872-C-T

http://identifiers.org/hco/10/GRCh38#125972985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133451897-C-A

125972985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133451897-C-T

125973175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133452074-G-C

125973199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133452106-A-G

125973463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 133452339-G-A

125973489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 133452365-G-A

125973489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 133452365-G-T

125973588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133452532-A-G

125973588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133452532-A-T

125974077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133453030-C-T

125974087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133453042-T-C

125974387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133453376-A-T

125974407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133453396-C-G

125974436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133453441-G-T

125974465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133453471-G-A

http://identifiers.org/hco/10/GRCh38#125979655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133454535-C-A

125979657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133454537-C-G

125979657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133454537-C-T

125979768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133454640-A-G

125979768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133454640-A-T

125979789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133454658-G-T

http://identifiers.org/hco/10/GRCh38#125979796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133454665-C-A

125979796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133454665-C-T

125979805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133454674-C-G

125979805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133454674-C-T

http://identifiers.org/hco/10/GRCh38#125979810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133454679-C-A

125979810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133454679-C-G

125979838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133454712-G-A

125979838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133454712-G-T

125979856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133454726-G-A

125979856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133454726-G-T

125980128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133454865-G-A

125980165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 133454899-C-T

125980226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 133454960-T-C

125980352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133455086-T-G

125980416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133455152-G-C

125980416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133455152-G-T

125980438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 133455182-A-G

125980646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133455354-G-T

125980729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133455437-T-A

125980729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133455437-T-C

125980729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133455437-T-G

125980793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133455499-G-A

125980793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133455499-G-C

125980793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133455499-G-T

http://identifiers.org/hco/10/GRCh38#125980884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133455572-C-A

125980884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133455572-C-T

125981714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133456014-C-T

125981737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133456035-G-A

125981762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133456053-A-G

125981885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133456170-A-G

125982221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133457972-T-C

125982399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133458138-C-G

125982399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133458138-C-T

125982566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133458299-A-G

http://identifiers.org/hco/10/GRCh38#125982907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133458601-A-C

125982907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133458601-A-T

http://identifiers.org/hco/10/GRCh38#125982932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133458626-A-C

125982932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133458626-A-G

125982932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133458626-A-T

125983031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133458732-T-C

125983242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133459035-C-T

125983300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133459081-C-T

125983325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133459105-T-C

125983368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133459147-C-T

125983379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133459158-G-A

125983389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133459168-C-T

125983461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133459242-G-A

125983517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133459300-G-A

125983687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133459399-G-A

125983687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133459399-G-C

125983748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133459455-T-A

125983904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133459600-C-T

125983968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133459664-A-G

125985431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133460126-A-T

125985455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133460147-T-C

125985768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133460371-G-A

125985913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133460472-G-C

125985999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133460558-G-C

125986202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133460750-G-A

125986533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133460984-C-T

125986616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133461065-C-T

125986701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133461103-C-T

http://identifiers.org/hco/10/GRCh38#125986712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133461114-C-A

125986721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133461123-G-C

125987232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133461486-G-A

125987355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133461608-C-T

http://identifiers.org/hco/10/GRCh38#125987451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133461680-C-A

125987453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133461682-A-G

125987650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133461862-G-T

125987755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133461956-C-G

125987819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133462012-T-C

125987824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133462017-C-G

125987903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133462149-C-T

125987941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133462185-C-G

125988009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133462251-G-A

125988011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133462253-G-T

125988087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133462328-A-G

125988183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133462422-G-T

125988208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133462446-A-T

125988212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133462450-A-G

125988310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: 133462532-T-C

http://identifiers.org/hco/10/GRCh38#125988360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133463427-A-C

125988543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 133463824-C-T

125988602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 133463883-C-T

http://identifiers.org/hco/10/GRCh38#125988662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133463943-A-C

125988662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 133463943-A-G

125988751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133464032-G-C

125988784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133464065-A-G

125988784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133464065-A-T

125988805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133464086-A-G

125988805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133464086-A-T

125988809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133464090-T-C

125988809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133464090-T-G

125988826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133464099-T-C

http://identifiers.org/hco/10/GRCh38#125988867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133464132-C-A

http://identifiers.org/hco/10/GRCh38#125988884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133464149-A-C

125988884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133464149-A-G

125988884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133464149-A-T

125988895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133464160-A-G

http://identifiers.org/hco/10/GRCh38#125988922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133464187-C-A

125988922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133464187-C-T

http://identifiers.org/hco/10/GRCh38#125988952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133464215-A-C

125988961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133464225-C-T

125990041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133464642-G-A

125990421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133464842-G-C

125990623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133465045-T-A

125991163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133465190-G-A

125991330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133465486-C-T

125991333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133465491-G-A

125991337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133465495-C-G

125991373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133465537-G-A

125991611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133465755-A-G

125991793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133465943-A-G

125992404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133466963-G-C

http://identifiers.org/hco/10/GRCh38#125992489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133467062-C-A

125992536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133467109-A-G

125992620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133467194-C-T

http://identifiers.org/hco/10/GRCh38#125992624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133467198-C-A

125992624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133467198-C-T

125992781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133467352-G-C

125994836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133469392-T-G

http://identifiers.org/hco/10/GRCh38#125995080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133469543-C-A

125995080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133469543-C-G

125995085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133469548-G-A

125995085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133469548-G-T

http://identifiers.org/hco/10/GRCh38#125995308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133469747-C-A

125995552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133470020-A-T

125995556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133470024-A-T

125995562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133470030-A-G

125995638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133470110-T-A

125995638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133470110-T-C

http://identifiers.org/hco/10/GRCh38#125995678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133470148-C-A

125995678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133470148-C-G

125995678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133470148-C-T

125995800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133470279-G-T

125995905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133470400-A-G

125996063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133470592-T-C

125996213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133470742-C-T

125996515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133470972-G-A

125996515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133470972-G-T

125996631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 133471092-C-T

http://identifiers.org/hco/10/GRCh38#125996680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133471133-C-A

125996680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133471133-C-G

125996811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133471232-C-G

125996811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133471232-C-T

125997069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133471450-A-G

125997145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133471527-A-G

125997319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133471663-G-C

125997319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133471663-G-T

125997396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133471728-T-C

125997512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133471845-G-A

125997512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133471845-G-T

125997554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133471882-A-G

125997850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133472078-C-T

http://identifiers.org/hco/10/GRCh38#125997852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133472080-C-A

125997852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133472080-C-T

125998028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133472201-G-A

125998193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133472399-G-T

125998580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133473002-C-G

125998650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133473071-G-C

125998800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133473225-A-G

125999018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133473505-T-G

125999107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133473595-T-A

125999107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133473595-T-C

http://identifiers.org/hco/10/GRCh38#126004505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133478096-C-A

126004505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133478096-C-T

126004515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133478106-A-G

126004537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133478122-G-A

126004584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133478168-G-A

126004584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133478168-G-T

126004650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133478237-A-T

http://identifiers.org/hco/10/GRCh38#126004681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133478268-C-A

126004681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133478268-C-G

http://identifiers.org/hco/10/GRCh38#126004686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133478273-C-A

126004686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133478273-C-G

http://identifiers.org/hco/10/GRCh38#126004716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133478312-C-A

126004716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133478312-C-G

126004716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133478312-C-T

126004770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133478369-A-G

126004832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133478426-G-T

126004838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133478432-G-C

126004838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133478432-G-T

126004841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133478435-G-T

http://identifiers.org/hco/10/GRCh38#126004873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133478466-A-C

126004873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133478466-A-G

126004875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133478468-A-G

126006861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133479562-A-G

126006997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133479717-G-A

126007057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133479776-T-C

126007141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133479856-A-G

126007328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133480033-C-G

126007332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133480037-T-C

126007513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133480186-A-G

126007527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133480200-C-G

http://identifiers.org/hco/10/GRCh38#126008621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133481794-C-A

126008621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133481794-C-T

126008667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133481843-G-A

126008667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133481843-G-T

126008910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133481921-G-A

126008910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133481921-G-T

126008950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133481943-G-A

126008950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133481943-G-T

http://identifiers.org/hco/10/GRCh38#126008962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133481955-C-A

126008962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133481955-C-T

126009044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133481992-T-G

http://identifiers.org/hco/10/GRCh38#126009163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133482097-C-A

126009170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133482100-G-A

126009170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133482100-G-C

http://identifiers.org/hco/10/GRCh38#126009528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133482480-C-A

126009528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23527
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133482480-C-T