http://identifiers.org/hco/10/GRCh38#69451471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62066998-C-A

69451501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 62066967-A-G

http://identifiers.org/hco/10/GRCh38#69451536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62066932-C-A

69451536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62066932-C-T

http://identifiers.org/hco/10/GRCh38#69451664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#62066823-C-A

69451664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 62066823-C-T

http://identifiers.org/hco/10/GRCh38#69451702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62066782-C-A

69451702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62066782-C-T

69451714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62066772-G-A

69451714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62066772-G-T

69451725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62066761-G-A

69451725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62066761-G-T

69451744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62066730-G-A

69451744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62066730-G-C

69451744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62066730-G-T

69451760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62066711-G-A

69451760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62066711-G-T

69451761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62066710-G-C

69451761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62066710-G-T

http://identifiers.org/hco/10/GRCh38#69451938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#62066516-C-A

69451938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62066516-C-T

69451976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62066467-C-T

69452163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62066293-G-A

69452240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62066219-A-T

69452574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62065993-T-C

69452717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62065312-G-T

69452749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62065280-C-G

69452951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62065072-T-C

69453253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62064792-A-G

69453401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62064655-C-G

69453401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62064655-C-T

69457129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62060194-G-A

69457129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62060194-G-C

69457129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62060194-G-T

69457406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62059948-C-T

69458311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62058139-C-T

69458975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62057624-G-A

69459407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62057281-A-G

69459451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62057237-A-T

69459892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62056762-C-T

69460285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62056114-G-A

69460285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62056114-G-C

69460298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62056097-C-T

69461235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62054972-G-A

69461348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62054865-G-A

69461454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62054761-G-A

69461454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62054761-G-C

69461797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62054478-G-C

http://identifiers.org/hco/10/GRCh38#69461928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62054388-C-A

69461928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62054388-C-G

69461928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62054388-C-T

http://identifiers.org/hco/10/GRCh38#69461934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62054382-A-C

http://identifiers.org/hco/10/GRCh38#69462153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62054262-A-C

69462156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62054259-T-G

69466012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62052859-G-A

69466127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62052745-A-G

69466875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62051376-T-C

69467126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62051082-G-T

69467301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62050905-A-G

69467349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62050857-G-A

69467349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62050857-G-T

69472761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62048557-C-T

69472853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62048483-G-A

69472940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62048403-G-A

69474671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62047550-C-G

69475003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62047271-A-G

69475093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62047130-C-G

69475148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62047079-T-G

http://identifiers.org/hco/10/GRCh38#69475177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62047046-C-A

http://identifiers.org/hco/10/GRCh38#69475309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62046955-C-A

69475652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62046699-C-T

69475829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62046529-T-G

69479136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62044896-C-G

69479323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62044715-T-C

69479368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62044667-G-C

http://identifiers.org/hco/10/GRCh38#69479439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62044616-C-A

69479472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62044590-G-T

69479481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62044581-A-G

69479495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62044567-T-C

69479501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62044561-C-T

69479516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62044546-C-T

69479517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62044545-C-T

69479776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62044289-C-T

69479883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62044203-C-G

69479929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62044149-G-A

69480048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62044002-C-G

69480067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62043980-C-T

69480255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62043808-G-A

69480332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62043708-G-A

69480422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62043627-G-A

69480499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62043548-G-A

69480504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62043543-C-T

69480537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62043510-T-A

69481468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62041996-C-T

69481729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62041781-C-G

69481729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62041781-C-T

69481847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62041676-C-G

69481848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62041675-C-T

69482211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62040316-C-G

69482300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62040235-G-T

69482330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62040213-C-T

69482587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62039972-G-A

69482820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62039761-C-T

69483000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62039665-G-C

69483000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62039665-G-T

69483001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62039664-T-C

69483175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62039545-A-G

69483226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62039478-G-A

69483292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62039441-G-T

69483324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62039406-T-A

69483488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62039289-T-C

69483588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62039169-G-A

69483588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62039169-G-T

69483709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62039024-C-G

69483709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 62039024-C-T

69483778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62038955-C-G

69483778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62038955-C-T

69483784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62038949-A-G

http://identifiers.org/hco/10/GRCh38#69483935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62038781-C-A

69483935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62038781-C-T

69483975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62038742-C-G

69483975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62038742-C-T

http://identifiers.org/hco/10/GRCh38#69483983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62038734-C-A

69484044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62038675-C-T

69484166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62038554-A-G

69484193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62038522-T-C

69484245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62038490-G-T

69484287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62038455-G-C

69484565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62038240-A-G

69484883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62037816-G-A

69484938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62037775-G-A

http://identifiers.org/hco/10/GRCh38#69485017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62037740-C-A

69485017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62037740-C-T

69485038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62037719-A-G

69485038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62037719-A-T

69485050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62037713-G-T

http://identifiers.org/hco/10/GRCh38#69485086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62037674-C-A

69485086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62037674-C-T

69485221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62037549-C-T

69485256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62037515-G-A

69485287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62037483-G-A

69485297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62037473-G-A

69485349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62037435-A-G

69485409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62037416-C-T

69485489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62037362-G-C

69485566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62037278-G-C

69485586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62037259-C-T

69485942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62036950-C-G

69486097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62036823-A-T

69486148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62036718-G-A

69486162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62036706-T-C

69486219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62036572-C-G

69486219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62036572-C-T

69486291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62036482-G-A

69486338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62036439-T-C

69486630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62036214-T-C

69486908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62035969-C-T

http://identifiers.org/hco/10/GRCh38#69486994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62035199-C-A

69486994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62035199-C-G

69486994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62035199-C-T

http://identifiers.org/hco/10/GRCh38#69487064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62035132-C-A

69487568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62035083-C-G

69487568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62035083-C-T

69487652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62035001-A-G

69487779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62034880-C-T

69488124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62033599-G-A

http://identifiers.org/hco/10/GRCh38#69488152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62033564-A-C

69488152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62033564-A-G

69488152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62033564-A-T

69488185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62033516-A-G

69488304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62033341-G-T

69488484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62033167-A-G

http://identifiers.org/hco/10/GRCh38#69489709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62033047-A-C

69489709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62033047-A-G

69489764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62032989-A-T

69489792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62032958-G-C

69491903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62032393-C-T

69492059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62032248-C-T

69492863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62031635-G-A

69492863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62031635-G-T

69492924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62031574-G-A

69492984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62031515-C-T

69493064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62031421-C-G

69493070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62031415-C-T

69493244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62031283-G-A

69493291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62031257-G-C

69494564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62030633-T-G

http://identifiers.org/hco/10/GRCh38#69494799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62030471-C-A

69494799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 62030471-C-T

69494829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 62030434-G-A

69494829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 62030434-G-T

http://identifiers.org/hco/10/GRCh38#69494976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62030307-C-A

69494976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62030307-C-T

69495052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62030216-T-C

http://identifiers.org/hco/10/GRCh38#69495103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62030125-C-A

69495103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62030125-C-T

69495299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62029958-G-A

69495299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62029958-G-T

http://identifiers.org/hco/10/GRCh38#69495351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62029912-A-C

69495351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62029912-A-G

69495351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62029912-A-T

69495420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62029906-G-A

69495420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62029906-G-T

69495423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 62029903-G-C

69495424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 62029902-G-A

69495424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 62029902-G-T

69495733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62029594-T-C

69495748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62029579-G-A

69495748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62029579-G-T

69496043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62029415-A-T

69496144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62029351-A-G

http://identifiers.org/hco/10/GRCh38#69496297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62029205-A-C

69497028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62028644-G-A

69497029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62028643-T-G

69497080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62028596-G-T

69497145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62028533-G-A

69497267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62028412-G-A

69497267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62028412-G-T

69497412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62028310-C-T

69497445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62028271-C-G

69497445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62028271-C-T

http://identifiers.org/hco/10/GRCh38#69497451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62028265-A-C

69497451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62028265-A-G

69497540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62028173-G-A

69497871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62027777-G-A

69498138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62027523-G-A

69498138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62027523-G-T

69498139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62027522-A-G

69498209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 62027431-G-T

69498217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 62027423-C-T

69498223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 62027417-G-A

69498223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 62027417-G-T

http://identifiers.org/hco/10/GRCh38#69498250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62027390-C-A

69498297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62027344-G-A

69498331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62027310-C-G

http://identifiers.org/hco/10/GRCh38#69498440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62027212-C-A

69498440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62027212-C-T

69498659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62027037-G-A

69498695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62027005-G-A

69498768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62026955-G-A

69498873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62026904-G-T

http://identifiers.org/hco/10/GRCh38#69499008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62026818-A-C

69499073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62026755-C-T

69499101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62026725-T-C

http://identifiers.org/hco/10/GRCh38#69499130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62026710-A-C

69503774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62026196-A-G

69503846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62026140-G-A

69503903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62026100-A-G

69504190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62025861-G-A

69504194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62025857-T-G

http://identifiers.org/hco/10/GRCh38#69504289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62025766-C-A

69504289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62025766-C-T

http://identifiers.org/hco/10/GRCh38#69504323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62025727-C-A

69504323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62025727-C-G

69504323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62025727-C-T

69504325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62025725-G-T

69504338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62025713-A-G

http://identifiers.org/hco/10/GRCh38#69504339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62025712-C-A

69504339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62025712-C-G

69504339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62025712-C-T

69504361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62025693-G-A

69504409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62025664-A-G

69504524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62025551-C-G

69504524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62025551-C-T

69504737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62025275-G-T

69504870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62025148-C-T

69505992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62024566-G-A

69506169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62024491-G-A

69506175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62024485-A-T

69506210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 62024450-G-A

69506210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 62024450-G-C

69506278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62024382-T-C

69506374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62024335-A-G

69506444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62024280-T-C

http://identifiers.org/hco/10/GRCh38#69506462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62024262-C-A

69506462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62024262-C-T

69506704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62024036-T-C

http://identifiers.org/hco/10/GRCh38#69506723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62024017-C-A

69506767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62024000-G-T

69506771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62023995-C-T

69506859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62023909-A-G

http://identifiers.org/hco/10/GRCh38#69506931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62023837-A-C

69506931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62023837-A-G

69506942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 62023826-G-A

http://identifiers.org/hco/10/GRCh38#69506970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62023798-C-A

69506970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62023798-C-T

http://identifiers.org/hco/10/GRCh38#69506983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62023769-C-A

69506983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62023769-C-T

69506995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62023757-G-A

69506995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62023757-G-T

69507032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62023720-A-G

69507049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62023707-T-C

http://identifiers.org/hco/10/GRCh38#69507085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62023667-C-A

69507103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62023649-G-A

69507103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62023649-G-T

69507140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62023613-C-G

69507190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62023602-T-C

http://identifiers.org/hco/10/GRCh38#69507214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62023586-C-A

http://identifiers.org/hco/10/GRCh38#69507230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62023570-C-A

69507230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62023570-C-T

http://identifiers.org/hco/10/GRCh38#69507239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62023561-C-A

69507239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62023561-C-G

http://identifiers.org/hco/10/GRCh38#69507339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62023452-C-A

69507339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62023452-C-T

69507375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62023437-G-A

69507375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62023437-G-T

http://identifiers.org/hco/10/GRCh38#69507428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62023382-C-A

69507428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62023382-C-T

http://identifiers.org/hco/10/GRCh38#69507441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62023369-C-A

69507441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62023369-C-T

69507496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62023315-T-C

69507496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62023315-T-G

http://identifiers.org/hco/10/GRCh38#69507611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62023190-C-A

http://identifiers.org/hco/10/GRCh38#69507767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#62023087-C-A

69507767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62023087-C-T

69507770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62023084-G-A

69507796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62023059-A-G

69507796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23298
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62023059-A-T