148697806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5 prime UTR variant
orthologous variants: 20421429-G-A

http://identifiers.org/hco/3/GRCh38#148697835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20421411-C-A

148697835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5 prime UTR variant
orthologous variants: 20421411-C-T

148697852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5 prime UTR variant
orthologous variants: 20421394-A-G

148697944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5 prime UTR variant
orthologous variants: 20421303-G-A

148697967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5 prime UTR variant
orthologous variants: 20421279-C-T

148697969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5 prime UTR variant
orthologous variants: 20421277-G-A

148697969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5 prime UTR variant
orthologous variants: 20421277-G-T

148697992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 20421259-G-C

148698056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5 prime UTR variant
orthologous variants: 20421237-A-G

http://identifiers.org/hco/3/GRCh38#148698117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20421206-C-A

148698117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5 prime UTR variant
orthologous variants: 20421206-C-T

http://identifiers.org/hco/3/GRCh38#148698123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#20421200-C-A

148698123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 20421200-C-T

148698135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 20421188-C-T

http://identifiers.org/hco/3/GRCh38#148698261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20421114-C-A

148698261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20421114-C-T

http://identifiers.org/hco/3/GRCh38#148698271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20421104-C-A

148698271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20421104-C-T

148698283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 20421093-G-T

148698310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20421067-A-G

148698310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20421067-A-T

148698311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20421066-G-A

148698341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20421047-G-T

148698445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20420988-T-C

148698479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20420965-C-G

148698857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20420639-G-T

148699057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20420502-G-C

http://identifiers.org/hco/3/GRCh38#148699093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20420458-C-A

148699093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20420458-C-G

148699093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20420458-C-T

148699103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20420448-C-T

148699143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20420395-G-A

148699315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20420224-G-A

148699449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20420089-T-G

148699627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20419920-T-C

148699829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20419427-T-C

148700168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20419127-T-C

148700168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20419127-T-G

148700398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20418921-T-C

148700437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20418889-T-A

148700872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20418484-T-G

148701487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20417595-T-A

148701654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20417334-G-A

148701705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20417293-G-A

148701705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20417293-G-C

http://identifiers.org/hco/3/GRCh38#148701710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20417288-A-C

148702514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20417010-T-G

148702595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20416939-C-T

148702779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20416739-C-G

148702789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20416729-T-A

148703003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20416515-G-A

148703187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20416118-T-A

148705482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20412638-A-G

148705617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20412511-G-A

148705630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20412497-G-A

148705684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20412465-C-G

http://identifiers.org/hco/3/GRCh38#148705813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20411946-C-A

148705813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20411946-C-T

148705814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20411945-C-T

148705933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20411824-A-G

148706538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20411661-G-A

148706831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20411410-T-C

148707818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20410465-G-A

148707972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20410327-T-C

148708053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20410253-G-T

http://identifiers.org/hco/3/GRCh38#148708057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20410249-C-A

148708118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20410154-T-C

148708130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20410142-A-G

148708131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20410141-G-T

148708169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20410103-A-G

148708256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20409442-C-G

148708259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20409439-T-G

http://identifiers.org/hco/3/GRCh38#148715753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20409038-C-A

148715808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20408985-T-A

148715808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20408985-T-C

http://identifiers.org/hco/3/GRCh38#148716136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20408625-C-A

148716278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20408495-T-G

148716345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20408002-A-G

148721059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20395495-G-A

148721103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20395445-C-T

148721115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20395433-T-C

148721148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20395400-C-T

148721267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20395293-T-C

148721267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20395293-T-G

148721432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20395136-T-C

148721589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20394966-T-G

148721671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20394891-G-A

148721701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20394868-G-A

148721727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20394835-C-T

148721989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20394705-A-T

http://identifiers.org/hco/3/GRCh38#148722062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20394633-C-A

148722412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20394363-T-G

148722713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20394104-C-T

148722750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20394069-C-T

http://identifiers.org/hco/3/GRCh38#148722798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20394018-A-C

148723096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20392748-A-G

148723247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20392590-C-T

148723415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20392459-A-T

148723582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20392302-A-G

http://identifiers.org/hco/3/GRCh38#148723689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20392190-C-A

148724430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20392036-C-G

148724474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20391996-T-C

148724548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20391935-T-C

148724769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20391773-A-G

148724983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20391574-C-T

148725936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20390609-G-A

148725936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20390609-G-T

148726055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20390286-C-T

148726124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20390209-C-G

148726509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20390078-C-T

148726542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20390051-G-A

148726583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20390014-T-G

148726598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20389999-G-A

http://identifiers.org/hco/3/GRCh38#148726755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20389879-A-C

148726779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20389851-G-A

148726885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20389749-T-G

http://identifiers.org/hco/3/GRCh38#148726886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20389748-A-C

148727009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20389577-A-G

148727372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20389123-C-T

http://identifiers.org/hco/3/GRCh38#148727459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#20389037-A-C

148727571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20388934-T-A

148727698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20388826-C-T

148727731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20388788-T-A

148727755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20388764-T-G

148728355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20388584-A-G

148728400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20388532-A-G

148728444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20388492-G-A

148728495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20388439-C-G

148728582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20388343-T-C

148728621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20388304-G-T

148728744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20388180-C-T

148728810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20388103-T-C

http://identifiers.org/hco/3/GRCh38#148728930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20387995-A-C

148729087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20387852-C-T

148729090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20387849-G-A

148729090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20387849-G-T

148729178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20387769-T-G

148729194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20387754-G-A

http://identifiers.org/hco/3/GRCh38#148729227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20387721-A-C

148729237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20387711-G-C

148729267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20387677-A-T

148729312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20387631-G-A

148729328-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20387611-T-A

148729427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20387485-T-G

148729616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20387298-A-T

148729928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20387005-A-G

http://identifiers.org/hco/3/GRCh38#148729950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20386980-C-A

148730035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20386911-G-T

148730105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20386847-G-A

148730105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20386847-G-T

148730292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20386681-C-G

148732115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20383656-T-C

148732238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20383537-G-A

148733155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20383058-C-T

148733513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20382720-C-G

148733513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20382720-C-T

148733538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20382518-C-T

148735648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20381173-G-A

148735648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20381173-G-C

148735748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20381063-G-T

http://identifiers.org/hco/3/GRCh38#148735901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20380926-A-C

148735901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20380926-A-T

148735934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20380900-A-T

148736032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20380743-G-T

148736034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20380741-T-C

148736094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20380666-G-A

148736249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20380529-A-T

148736302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20380492-A-G

148736302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20380492-A-T

148736390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20380406-G-T

148736938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20379625-T-C

148736979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20379584-C-T

148737083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20379502-A-T

148737197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20378880-C-G

148737322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20378758-A-G

http://identifiers.org/hco/3/GRCh38#148737381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20378692-A-C

148737381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20378692-A-T

http://identifiers.org/hco/3/GRCh38#148737422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20378614-A-C

148737443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20378593-A-G

148737598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20378469-G-A

148737625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20378314-G-A

148737765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20377960-G-A

148737771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20377954-G-A

148737870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20377853-C-G

148737870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20377853-C-T

148738033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20377673-T-C

148738057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20377657-G-T

http://identifiers.org/hco/3/GRCh38#148738058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20377656-C-A

148738059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20377655-T-C

148738222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20377506-A-G

148738309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20377431-G-A

148738403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20377336-G-A

148739450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20371978-G-T

148739516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20371909-T-C

http://identifiers.org/hco/3/GRCh38#148739519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20371857-A-C

148739584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20371783-T-G

148739592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20371775-C-T

148739735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20371675-A-G

148739798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_acceptor_variant
orthologous variants: 20371612-A-G

148739829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 20371589-A-G

148739829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 20371589-A-T

http://identifiers.org/hco/3/GRCh38#148739928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20371513-C-A

http://identifiers.org/hco/3/GRCh38#148739931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20371510-C-A

148739937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 20371504-G-T

http://identifiers.org/hco/3/GRCh38#148739943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20371498-C-A

http://identifiers.org/hco/3/GRCh38#148739964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20371477-C-A

148740119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20371328-A-G

148740129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20371318-A-G

148740168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20371280-C-T

148740174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20371274-C-T

148740228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20371224-A-T

148740280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20371160-A-G

148740652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20370826-A-G

148740886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20370734-T-C

148740887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20370733-A-G

148740887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20370733-A-T

148740900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20370720-T-G

148740964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: intron variant
orthologous variants: 20370659-A-G

148741023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 5 prime UTR variant
orthologous variants: 20370619-C-T

148741154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: missense variant
orthologous variants: 20370484-T-C

148741297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: missense variant
orthologous variants: 20370341-A-G

148741354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: missense variant
orthologous variants: 20370284-A-G

148741384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: missense variant
orthologous variants: 20370254-T-C

148741417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: synonymous variant
orthologous variants: 20370221-C-T

148741450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: stop gained
orthologous variants: 20370188-C-T

148741604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: missense variant
orthologous variants: 20370034-C-G

148741777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: missense variant
orthologous variants: 20369861-T-C

http://identifiers.org/hco/3/GRCh38#148741848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20369790-A-C

148741897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: missense variant
orthologous variants: 20369741-A-G

http://identifiers.org/hco/3/GRCh38#148741958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20369680-A-C

148742117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20369520-A-G

http://identifiers.org/hco/3/GRCh38#148742142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20369495-A-C

http://identifiers.org/hco/3/GRCh38#148742151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20369486-A-C

148742151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20369486-A-G

148742208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20369419-A-G

148742242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20369387-G-A

148742340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20369259-T-C

148742340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20369259-T-G

148742347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20369252-A-G

148742351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20369248-C-T

http://identifiers.org/hco/3/GRCh38#148742357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20369242-C-A

148742463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20369131-G-A

148742478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20369116-T-A

148742500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20369093-G-A

http://identifiers.org/hco/3/GRCh38#148742550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20369056-C-A

148742550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20369056-C-T

http://identifiers.org/hco/3/GRCh38#148742558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20369050-C-A

148742558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20369050-C-T

http://identifiers.org/hco/3/GRCh38#148742585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20369023-C-A

148742585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20369023-C-T

148742664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20368944-T-A

148742664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20368944-T-C

148742664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20368944-T-G

148742665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20368943-G-A

148742665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20368943-G-C

148742665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20368943-G-T

148742667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20368941-G-T

148742678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20368931-T-G

148742735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20368868-G-A

148742735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20368868-G-T

148742801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20368816-G-A

148742894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 336
most severe consequence: 3 prime UTR variant
orthologous variants: 20368730-A-G