70259007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 5 prime UTR variant
orthologous variants: 23251242-G-A

70259007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 5 prime UTR variant
orthologous variants: 23251242-G-T

70259042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 23251217-G-A

70259060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 5 prime UTR variant
orthologous variants: 23251199-G-A

70259103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense_variant, undefined
orthologous variants: 23251156-T-C

http://identifiers.org/hco/9/GRCh38#70259106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#23251153-A-C

70259106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense_variant, undefined
orthologous variants: 23251153-A-G

70259328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, undefined
orthologous variants: 23250937-G-A

70259328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, undefined
orthologous variants: 23250937-G-C

http://identifiers.org/hco/9/GRCh38#70259335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#23250930-C-A

70259335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, undefined
orthologous variants: 23250930-C-G

70259335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, undefined
orthologous variants: 23250930-C-T

70259887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23250481-A-T

70261197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23249973-G-A

70261210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23249961-C-G

http://identifiers.org/hco/9/GRCh38#70261212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23249959-A-C

70261232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23249939-C-T

http://identifiers.org/hco/9/GRCh38#70261247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23249926-C-A

70261443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23249786-C-T

70261605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23249612-G-C

70261889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23249051-T-C

70263410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23247612-T-C

70263759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23247087-A-G

70264178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23246384-A-T

http://identifiers.org/hco/9/GRCh38#70264184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23246377-A-C

70264192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23246369-T-G

70264230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23246331-G-A

70264230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23246331-G-T

70264311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense variant
orthologous variants: 23246223-G-A

70264401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense variant
orthologous variants: 23246133-C-G

70266208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23245115-A-G

70266320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23245013-C-G

70266341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23244992-A-G

70266548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23244805-C-T

70266734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23244624-T-C

70266792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23244565-T-G

70266869-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23244504-T-G

70267260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23243652-A-G

70267471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23243458-A-G

70267481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23243448-C-T

70267500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23243430-C-T

70267538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23243392-C-G

70267620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23243346-A-G

70267839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23243167-G-T

70267867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23243136-G-A

70267867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23243136-G-T

70267885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23243118-G-A

70267908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23243094-T-C

http://identifiers.org/hco/9/GRCh38#70268062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23242948-A-C

70268062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23242948-A-G

70276701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 23242473-G-C

70276911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23241952-G-A

70277314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 23241124-A-T

http://identifiers.org/hco/9/GRCh38#70277341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23241097-C-A

70277341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 23241097-C-G

70277341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 23241097-C-T

70277344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 23241094-G-C

70277510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23240927-T-A

70277510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23240927-T-C

70277518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23240919-G-A

70277522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23240915-C-G

70278365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23238935-A-G

70278365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23238935-A-T

70278381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23238919-T-C

70278397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23238905-T-A

70278397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23238905-T-C

70278397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23238905-T-G

70278429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23238887-A-T

70278439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23238877-A-G

70278660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23238659-T-C

70278740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23238432-T-G

70278741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23238431-T-C

70278816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23238356-A-T

70278818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23238354-G-C

70278897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23238300-A-G

70278956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23238247-G-C

70279851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23238079-T-C

70280336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23237649-A-G

70280652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23237255-A-T

70280710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23237199-G-C

70280710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23237199-G-T

70282390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23235043-C-T

70282409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23235024-A-G

70282524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23234909-T-C

70282551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23234882-C-G

70282551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23234882-C-T

70282552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23234881-G-A

70282553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23234880-T-C

70282591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 23234842-T-C

70282651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23234786-G-A

70282651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23234786-G-C

70282725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23234718-A-G

70282725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23234718-A-T

70282760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23234671-G-T

70282880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23234514-A-G

70284455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23233130-A-G

70284640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23232956-T-C

70284779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23232807-T-C

70284923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23232677-G-A

70284951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23232648-A-G

70284951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23232648-A-T

70285936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23232398-T-C

http://identifiers.org/hco/9/GRCh38#70285939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23232395-A-C

70286034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23232284-T-C

70286056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23232264-G-A

70286056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23232264-G-T

70286132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23232172-G-A

70286132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23232172-G-C

70286132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23232172-G-T

70286218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23232092-G-A

70286218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23232092-G-C

70286218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23232092-G-T

70286311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23232002-G-T

70286351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23231972-T-C

70286366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23231947-G-A

70286366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23231947-G-T

http://identifiers.org/hco/9/GRCh38#70286374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23231939-C-A

http://identifiers.org/hco/9/GRCh38#70286375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23231938-C-A

70286375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23231938-C-T

http://identifiers.org/hco/9/GRCh38#70286396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23231904-A-C

70286414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23231886-T-G

70293935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23225227-T-C

70294062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23225125-T-G

70294087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23225113-A-T

70295538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23223910-C-T

70295617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23223838-G-C

70295727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23223724-C-G

70295763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23223692-A-G

70296710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23222979-T-G

70296712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23222977-T-C

70296771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23222919-G-A

70296771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23222919-G-C

70297652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23222447-A-G

70297652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23222447-A-T

70297889-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23221547-A-T

70297912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23221524-T-A

70297912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23221524-T-C

70297930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23221506-A-G

70298038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense variant
orthologous variants: 23221400-A-G

70298114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense variant
orthologous variants: 23221324-A-G

70298186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense variant
orthologous variants: 23221252-G-A

70298230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23221208-C-T

70298247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23221193-A-G

70298275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23221165-T-C

70299576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23220630-T-C

70299906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23220261-A-G

70299906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23220261-A-T

http://identifiers.org/hco/9/GRCh38#70300009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23220183-C-A

70300209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23219989-C-T

http://identifiers.org/hco/9/GRCh38#70300298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23219892-C-A

70300309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23219878-T-A

http://identifiers.org/hco/9/GRCh38#70301041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23218962-A-C

70301390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23218520-A-G

70301474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23218449-C-T

http://identifiers.org/hco/9/GRCh38#70301487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23218437-C-A

70301487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23218437-C-G

70301552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23218380-T-G

70301602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23218336-A-G

70301603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23218335-T-C

70304786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23216898-C-G

http://identifiers.org/hco/9/GRCh38#70304941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23216765-A-C

70304981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23216736-A-G

70305018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23216700-A-G

70305213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23216396-A-G

http://identifiers.org/hco/9/GRCh38#70305373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23216234-C-A

70314065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23214061-G-T

70314094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23214045-T-C

http://identifiers.org/hco/9/GRCh38#70314293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23213857-A-C

70314308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23213842-C-G

70314464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23213715-A-T

70314642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23213425-T-C

70314668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23213400-G-T

70314670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23213398-A-G

70314795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: synonymous variant
orthologous variants: 23213277-A-G

http://identifiers.org/hco/9/GRCh38#70314849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23213222-A-C

70314849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23213222-A-G

70314849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23213222-A-T

70314915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23213151-G-A

70314915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23213151-G-T

70314917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23213149-T-C

http://identifiers.org/hco/9/GRCh38#70315447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23211456-C-A

70315447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: splice_region_variant, stop_gained
orthologous variants: 23211456-C-T

70317582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23209967-G-A

70317755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23209821-G-A

70317755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23209821-G-C

70318407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23209469-T-A

70318407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23209469-T-G

70318484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23209384-A-G

70318530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense variant
orthologous variants: 23209338-G-A

70318530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense variant
orthologous variants: 23209338-G-T

http://identifiers.org/hco/9/GRCh38#70318682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23209186-C-A

70318682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense variant
orthologous variants: 23209186-C-G

70318682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: synonymous variant
orthologous variants: 23209186-C-T

70318767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23209116-T-C

70318834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense variant
orthologous variants: 23209049-T-G

70318848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense variant
orthologous variants: 23209035-A-T

70318969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23208914-T-G

70319061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23208839-T-A

70319061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23208839-T-G

70319093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23208810-C-T

70322481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23207396-A-G

70323445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23206442-T-G

70323453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23206434-G-A

70323528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: synonymous variant
orthologous variants: 23206355-G-A

70323603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23206280-A-G

70323679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23206203-G-A

70323679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23206203-G-T

70323747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23206128-T-C

70323903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23205794-G-T

70323904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23205793-G-T

70323920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23205778-A-G

70324033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23205646-T-C

70324271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23205407-A-G

http://identifiers.org/hco/9/GRCh38#70324930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23204655-A-C

http://identifiers.org/hco/9/GRCh38#70324983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23204611-C-A

70325162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23204459-T-A

70342417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23198900-T-C

http://identifiers.org/hco/9/GRCh38#70342516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23198795-A-C

70342696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23198627-A-G

70342717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23198606-G-A

70342789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23198535-A-G

70343263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23196389-G-A

70343998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23196039-A-G

http://identifiers.org/hco/9/GRCh38#70344096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23195934-C-A

http://identifiers.org/hco/9/GRCh38#70344147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23195889-C-A

70344147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23195889-C-T

70344165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23195871-G-A

70344165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 23195871-G-T

70344209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23195827-A-G

70344237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23195799-G-A

70344237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23195799-G-T

70344240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23195796-G-A

70344240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 23195796-G-T

70344257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23195779-A-G

70344274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23195762-G-A

70344274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23195762-G-T

70344283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23195754-G-A

70344283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23195754-G-C

70344283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23195754-G-T

http://identifiers.org/hco/9/GRCh38#70344293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23195744-C-A

70344293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23195744-C-T

http://identifiers.org/hco/9/GRCh38#70344296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23195741-C-A

70344296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23195741-C-G

70344296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23195741-C-T

70344304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23195733-A-G

70344307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23195730-T-C

70344315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23195722-T-A

70344315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23195722-T-C

70344318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23195719-T-C

70344329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23195708-A-G

70344525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23195462-T-C

70344590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23195395-G-C

70344590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23195395-G-T

70344681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23195306-A-G

http://identifiers.org/hco/9/GRCh38#70344772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23195225-C-A

70344772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23195225-C-T

http://identifiers.org/hco/9/GRCh38#70345057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23194955-A-C

70345057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23194955-A-G

70345176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23194788-T-C

70345202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23194729-A-T

70346000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23193161-A-G

70346000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23193161-A-T

70346020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23193141-A-G

70346020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23193141-A-T

70346079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23193099-A-G

70346297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23192869-A-T

70346306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23192860-T-A

70346306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23192860-T-C

70346306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: 23192860-T-G

http://identifiers.org/hco/9/GRCh38#70346334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23192822-C-A

http://identifiers.org/hco/9/GRCh38#70346382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23192777-A-C

http://identifiers.org/hco/9/GRCh38#70346417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23192742-A-C

70346423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23192738-G-A

70346423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23192738-G-T

70346450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23192711-A-G

70346491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23192675-A-T

70346494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23192672-T-C

http://identifiers.org/hco/9/GRCh38#70346703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23192464-C-A

70346932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23192235-T-C

http://identifiers.org/hco/9/GRCh38#70347234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23191896-C-A

70347234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23191896-C-T

70347339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23191793-A-G

http://identifiers.org/hco/9/GRCh38#70347508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23191630-C-A

70347508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23191630-C-T

70347539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23191600-A-G

70347539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23191600-A-T

70347768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23191388-G-T

70348046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 23191107-T-C

70348047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23191106-G-A

70348047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23191106-G-T

70348056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23191097-A-T

70348140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23191023-A-G

70348161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23190999-G-T

http://identifiers.org/hco/9/GRCh38#70348183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23190977-C-A

70348183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23190977-C-G

70348183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23190977-C-T

70348279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23190877-G-T

http://identifiers.org/hco/9/GRCh38#70350466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23187618-C-A

http://identifiers.org/hco/9/GRCh38#70350499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23187586-C-A

70350499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23187586-C-T

http://identifiers.org/hco/9/GRCh38#70350598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23187487-C-A

70350598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23187487-C-G

70352146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23186379-T-C

70352178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23186343-T-G

70352227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23186294-G-A

70352352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 3 prime UTR variant
orthologous variants: 23186168-T-C

70352409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 3 prime UTR variant
orthologous variants: 23186104-G-A

70352409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 3 prime UTR variant
orthologous variants: 23186104-G-T

70352453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 3 prime UTR variant
orthologous variants: 23186058-A-G

70352464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 3 prime UTR variant
orthologous variants: 23186047-G-T

70352542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 3 prime UTR variant
orthologous variants: 23185976-A-G

70352556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 3 prime UTR variant
orthologous variants: 23185962-G-A

70352556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 3 prime UTR variant
orthologous variants: 23185962-G-T

http://identifiers.org/hco/9/GRCh38#70352557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23185961-C-A

70352557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 3 prime UTR variant
orthologous variants: 23185961-C-T

http://identifiers.org/hco/9/GRCh38#70352808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23185619-C-A

70352808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 3 prime UTR variant
orthologous variants: 23185619-C-T

70352972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 3 prime UTR variant
orthologous variants: 23185481-T-C

70353007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 3 prime UTR variant
orthologous variants: 23185451-A-G

70353087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 3 prime UTR variant
orthologous variants: 23185385-G-T

70353233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 3 prime UTR variant
orthologous variants: 23185216-A-G

70353233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 3 prime UTR variant
orthologous variants: 23185216-A-T

70353300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 3 prime UTR variant
orthologous variants: 23185152-G-T

http://identifiers.org/hco/9/GRCh38#70354858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23183833-C-A

70354858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20465
most severe consequence: 3 prime UTR variant
orthologous variants: 23183833-C-T