95116911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, undefined
orthologous variants: 121057039-G-A

95116943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121056999-A-G

95117050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, undefined
orthologous variants: 121056894-T-G

http://identifiers.org/hco/1/GRCh38#95117261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121056679-C-A

95117342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121056598-C-T

http://identifiers.org/hco/1/GRCh38#95117436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121056507-C-A

95117436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121056507-C-T

95117461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121056499-G-T

http://identifiers.org/hco/1/GRCh38#95117589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#121056373-C-A

95117589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 121056373-C-T

95117710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121056293-A-G

95117716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121056287-G-A

95117746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121056258-G-A

95117874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, undefined
orthologous variants: 121056167-G-T

http://identifiers.org/hco/1/GRCh38#95117988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121056051-C-A

95117988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121056051-C-T

95117989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121056050-G-A

95117989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121056050-G-T

95118050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121055990-C-T

95118063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121055977-G-A

95118063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121055977-G-C

http://identifiers.org/hco/1/GRCh38#95118064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121055976-C-A

95118064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121055976-C-T

http://identifiers.org/hco/1/GRCh38#95118065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121055975-C-A

95118278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121055782-C-T

95118385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121055670-A-G

95118487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121055577-T-C

95118528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121055532-G-A

95118893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121055218-C-T

95119286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121054853-G-A

95119861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121054327-T-C

95120017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121054175-G-T

95120044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121054137-C-T

95120088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121054093-G-A

95120088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121054093-G-T

95120160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121054018-G-T

http://identifiers.org/hco/1/GRCh38#95120369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121053843-A-C

95120503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121053719-C-T

95120512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121053710-G-C

95120603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121053621-G-A

95120784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121053467-A-G

95120840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121053412-T-G

95120945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121053340-G-A

95120945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121053340-G-T

95120949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121053336-T-C

95120985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121053317-G-T

95121008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121053294-G-T

http://identifiers.org/hco/1/GRCh38#95121295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121053001-C-A

95121295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121053001-C-T

95121323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121052955-G-A

95121323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121052955-G-T

95121410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121052872-C-T

95121797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121052791-A-G

95121920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121052709-T-G

95121936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121052693-G-A

95121950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121052679-G-T

95122531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121052426-A-G

95122585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121052373-C-T

95122796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121052215-T-C

95122811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121052200-T-G

95122813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121052198-A-G

95124223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121050447-G-A

http://identifiers.org/hco/1/GRCh38#95124540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121049995-C-A

95124716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121049836-T-C

95124718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121049834-C-T

95125705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121047625-A-G

95127211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121045136-A-G

95127295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121045077-A-G

95127396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121044971-G-C

95127469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121044886-A-G

95127668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121044704-G-C

95127668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121044704-G-T

95127680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121044692-A-G

95127873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121044513-A-G

95128111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121042937-G-C

95128319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121042745-G-A

http://identifiers.org/hco/1/GRCh38#95128383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121042673-A-C

95128387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121042669-T-G

95128434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121042077-A-G

95129235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121041358-C-T

95136212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121035064-A-G

95136212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121035064-A-T

http://identifiers.org/hco/1/GRCh38#95136354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121034952-C-A

95136908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121034549-G-T

95136954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121034505-G-A

95137117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121034355-G-A

95137163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121034313-G-A

95137235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121034250-G-A

95140514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121033188-T-G

95140524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121033178-T-A

http://identifiers.org/hco/1/GRCh38#95140659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121033053-C-A

http://identifiers.org/hco/1/GRCh38#95140689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121033023-C-A

95141476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121031154-T-A

95141482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121031150-C-T

95141705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121030964-C-T

95141800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121030863-C-T

95141843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121030823-G-A

95141843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121030823-G-T

95141960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121030703-T-C

95142123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121030554-T-G

95142155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121030387-A-T

95142174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121030366-G-C

95142175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121030365-A-G

95142202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121030337-T-C

95143745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121029054-G-A

95143745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121029054-G-C

95143745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121029054-G-T

95143754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121029045-T-C

95143774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121029018-A-T

http://identifiers.org/hco/1/GRCh38#95143815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121028974-C-A

95143815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121028974-C-T

95143862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121028922-C-T

95143884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121028900-T-C

http://identifiers.org/hco/1/GRCh38#95143913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121028833-C-A

95143913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121028833-C-T

95143926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121028820-A-G

95143926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121028820-A-T

95144028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121028718-T-C

95144102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121028642-A-G

95144132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121028628-G-A

95144132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121028628-G-T

95145681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121027883-C-T

95145758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121027805-G-A

95145820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121027733-T-C

95145833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121027694-A-G

95147549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121026678-C-T

95147598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121026627-A-G

95148146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121025787-T-C

http://identifiers.org/hco/1/GRCh38#95148156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121025782-A-C

95148222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121025718-C-T

95148233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121025707-C-T

95148490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121025251-A-G

http://identifiers.org/hco/1/GRCh38#95148572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121025094-C-A

95148572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121025094-C-G

95148572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121025094-C-T

95148576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121025092-G-A

95148576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121025092-G-T

95148675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121024999-C-T

95148784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121024888-C-G

95148784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121024888-C-T

http://identifiers.org/hco/1/GRCh38#95148819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121024855-C-A

95149170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121024520-T-C

95149172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121024518-T-G

95149455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121024256-T-C

95149595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121024113-T-C

95149623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121024085-T-C

95149677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121024037-A-T

95149681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121024031-T-C

95149719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121023998-A-T

95150363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121022402-T-C

95150363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121022402-T-G

95150367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121022398-A-G

http://identifiers.org/hco/1/GRCh38#95150381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121022384-C-A

95151188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121022178-A-G

95151198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121022169-G-T

95151216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121022157-G-A

95151216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121022157-G-T

95151242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121022130-G-T

95151392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: synonymous variant
orthologous variants: 121021984-G-A

http://identifiers.org/hco/1/GRCh38#95151446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121021894-A-C

95151503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121021842-A-G

95151504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121021841-A-G

95152252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121019950-C-T

95152260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121019942-A-G

95152281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121019915-C-T

95152430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121019796-T-A

95152518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121019729-G-A

95152557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121019686-C-T

95156268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121013519-G-A

95156284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121013503-A-G

95156294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121013493-A-G

95156301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121013486-G-C

95156409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121013349-A-G

95156421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121013337-C-T

95156470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121013302-G-T

95156482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron variant
orthologous variants: 121013290-A-G

95169417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121011566-T-C

95169875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121011320-G-T

95169961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121010992-T-C

95169994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121010958-A-G

95171036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121009642-T-C

95171340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121009508-C-T

95171342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121009506-G-A

95171440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121009398-T-C

95171933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121008989-C-T

95172101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121008844-T-C

95172970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121005889-C-T

95173110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121005718-C-T

95173194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121005636-G-A

95173212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121005618-A-G

95173666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121005129-T-C

http://identifiers.org/hco/1/GRCh38#95173667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121005128-C-A

95173837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121004997-A-G

95173837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121004997-A-T

95174015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121004832-A-G

http://identifiers.org/hco/1/GRCh38#95174016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121004831-C-A

95174018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121004829-A-G

95174018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121004829-A-T

95174026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121004821-A-G

95177327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121003687-T-C

95177340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121003677-G-A

95177340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121003677-G-C

95177396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121003627-A-T

95177459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121003564-T-C

95191744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121000923-G-T

95191871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121000796-G-C

95191871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121000796-G-T

95191919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121000735-T-A

95191948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121000717-A-G

95191948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121000717-A-T

95192544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121000434-G-A

95192544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121000434-G-T

http://identifiers.org/hco/1/GRCh38#95192614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121000374-A-C

95192727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121000262-A-G

95192833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121000173-A-G

95193237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120999824-A-G

95193241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120999820-A-G

95193329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120999746-T-C

95193829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120999215-G-T

95193848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120999192-G-A

95194132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120998909-T-G

95194263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120998814-A-T

95194328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120998766-A-G

95194525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120998575-A-G

95194525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120998575-A-T

95194985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120998137-G-A

95195138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120997992-T-C

95195150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120997980-C-T

95195250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120997891-G-A

95195250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120997891-G-T

95195259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120997888-G-T

95195683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120997440-C-T

http://identifiers.org/hco/1/GRCh38#95195733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#120997394-C-A

95195733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120997394-C-T

95195762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120997365-A-G

http://identifiers.org/hco/1/GRCh38#95195764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#120997363-C-A

http://identifiers.org/hco/1/GRCh38#95195773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#120997354-C-A

95196014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120997117-A-G

95196014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120997117-A-T

95196108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120997026-A-G

95196125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120997009-G-A

95196311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120996833-T-C

95196311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120996833-T-G

95196315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120996829-A-G

95196334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120996815-G-A

95196779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120996417-C-T

http://identifiers.org/hco/1/GRCh38#95197017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#120996180-A-C

95197168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120996083-A-G

http://identifiers.org/hco/1/GRCh38#95197234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#120996014-A-C

95197592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26477
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120995670-A-G