103120200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97697855-G-T

103120213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97697842-G-A

103120213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97697842-G-T

103120271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97697783-G-A

103120271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97697783-G-T

103120273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97697781-G-A

103120273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97697781-G-T

103120311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97697741-G-A

103120342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97697726-C-G

103120342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97697726-C-T

103120375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97697692-T-C

103120403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97697664-T-C

103120448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 97697617-C-T

103120452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 97697613-C-T

103120455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 97697611-A-G

103120547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97697534-A-G

http://identifiers.org/hco/5/GRCh38#103120659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97697417-C-A

103120659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97697417-C-T

103120847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97697231-A-G

http://identifiers.org/hco/5/GRCh38#103120887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97697207-C-A

103120887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97697207-C-T

103120942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97697136-G-T

103121097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97696995-T-C

http://identifiers.org/hco/5/GRCh38#103121136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97696947-C-A

103121156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97696933-G-A

103121156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97696933-G-T

103121210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97696889-T-G

103121416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97696696-G-A

103121416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97696696-G-T

103121590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97696547-G-A

103121590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97696547-G-T

103121752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97696379-C-T

103121753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97696378-A-G

103122196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97696271-G-A

103122409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97696069-C-G

103122444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97696000-A-G

103122848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97695591-T-A

103122876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97695563-C-T

103123202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97695245-G-T

103123849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97694683-T-A

103123897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97694636-T-C

103124832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97694024-A-T

103124981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97693885-C-T

103125066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97693815-C-G

103125486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97692410-G-T

103125488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97692408-A-G

103125488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97692408-A-T

103126098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97692108-C-T

103126116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97692091-T-C

103127383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97691315-A-G

103127490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97691281-A-G

103127597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97691177-G-A

103127597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97691177-G-T

103127676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97691108-G-T

103128038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97690421-T-A

103128125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97690350-C-G

103128187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97690290-T-C

103128574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97690120-G-C

103128603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97690096-C-T

103128710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97689993-A-G

103129032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97689784-T-A

103129084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97689737-G-A

103129194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97689654-A-G

103129297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97689553-G-T

http://identifiers.org/hco/5/GRCh38#103129369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97689478-C-A

103129369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97689478-C-T

103129422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97689425-T-A

103129531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97689319-A-G

103129531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97689319-A-T

103129572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97689279-A-G

103129620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 97689231-C-T

103129674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 97689177-G-A

103129683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 97689168-G-A

103129683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 97689168-G-T

103129749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97689113-T-C

103129810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97689080-A-G

103130016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97688963-A-G

103130037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97688942-G-A

103130086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97688914-A-G

103133086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97687598-A-G

103133361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97687178-T-A

103133365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97687174-T-A

103133365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97687174-T-C

103133416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97687124-A-G

103133597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 97686943-C-G

103133597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 97686943-C-T

103133651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97686889-A-G

103133652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97686888-T-A

103133721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97686823-T-C

http://identifiers.org/hco/5/GRCh38#103134364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97686212-A-C

103134474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97686115-A-T

103134514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97686099-T-C

http://identifiers.org/hco/5/GRCh38#103134600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97686028-C-A

103134600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97686028-C-T

103135047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97685640-C-T

103135963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97685089-T-C

103136629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97684764-A-G

103136679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97684709-A-G

103136871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97684520-T-C

103136872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97684519-T-A

103136872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97684519-T-G

103136890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97684501-G-A

103136890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97684501-G-T

103137060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97684371-G-A

103137060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97684371-G-C

103146492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97682967-A-G

103146731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97682720-T-C

http://identifiers.org/hco/5/GRCh38#103146778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97682667-C-A

103146778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97682667-C-T

103146871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97682115-G-A

103146943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97682044-C-G

103146996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97681990-A-G

103147501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97681112-T-C

http://identifiers.org/hco/5/GRCh38#103147604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97681014-A-C

103147863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97680598-G-A

http://identifiers.org/hco/5/GRCh38#103147897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97680563-C-A

103148034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: splice donor variant
orthologous variants: 97680425-T-C

103148278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97679268-A-G

103148339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97679210-A-G

103148342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97679207-A-T

103148492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97679073-C-G

103148558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97679001-A-G

103148694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97678878-C-T

103148800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97678754-T-C

103148975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97678654-T-C

103149009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97678620-A-G

103149092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97678511-T-A

103149108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97678495-A-G

103149134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97678469-A-G

103149343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97678259-T-C

103149383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97678225-T-A

103149390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97678219-G-A

103149434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97678176-G-T

103149631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97677965-G-A

103149681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97677888-G-C

103150084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97677799-T-C

http://identifiers.org/hco/5/GRCh38#103150240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97677643-A-C

103151710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97676985-T-C

103151997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97676749-C-T

http://identifiers.org/hco/5/GRCh38#103152611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97675407-C-A

103152611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97675407-C-T

103152652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: missense variant
orthologous variants: 97675367-A-G

103152652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: missense variant
orthologous variants: 97675367-A-T

http://identifiers.org/hco/5/GRCh38#103152869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97675147-C-A

103153402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97674581-A-G

103153834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97674260-T-C

103153867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: missense variant
orthologous variants: 97674208-A-T

http://identifiers.org/hco/5/GRCh38#103153954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97674122-A-C

103153954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97674122-A-G

103153958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97674119-A-G

http://identifiers.org/hco/5/GRCh38#103153960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97674117-C-A

103153960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97674117-C-G

103153960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97674117-C-T

http://identifiers.org/hco/5/GRCh38#103153971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97674110-C-A

103153971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97674110-C-G

103154003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97674080-T-C

103154003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97674080-T-G

103154140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97673944-A-G

103154432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97673693-A-G

103154659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97673204-T-A

103154665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 97673198-A-G

103154665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 97673198-A-T

103154677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: missense variant
orthologous variants: 97673186-G-T

103154819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97673012-T-C

http://identifiers.org/hco/5/GRCh38#103154864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97672965-A-C

103154864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: missense variant
orthologous variants: 97672965-A-G

103154864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: missense variant
orthologous variants: 97672965-A-T

103154939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: missense variant
orthologous variants: 97672890-G-C

http://identifiers.org/hco/5/GRCh38#103155233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97672687-C-A

103155278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97672649-T-C

103155278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97672649-T-G

103155854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97671944-G-A

103155878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97671898-G-A

103158199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: missense variant
orthologous variants: 97668907-G-C

103158342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97668770-C-T

103158577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97668543-T-C

103159070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97668440-A-T

http://identifiers.org/hco/5/GRCh38#103159170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97668343-C-A

103159269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: missense variant
orthologous variants: 97668244-G-A

103159269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: missense variant
orthologous variants: 97668244-G-T

103164843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97663187-G-T

103164881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97663151-A-G

103167139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97662871-G-A

103167139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97662871-G-T

103167144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97662866-A-G

http://identifiers.org/hco/5/GRCh38#103167201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97662809-C-A

103167291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: missense variant
orthologous variants: 97662719-G-A

103167291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: missense variant
orthologous variants: 97662719-G-T

103167329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97662681-G-T

103167443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97662579-G-C

103167469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97662567-T-C

103167482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97662554-A-G

103168012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97661892-A-G

103168012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97661892-A-T

103168041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97661863-T-C

103168212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: stop gained
orthologous variants: 97661692-C-T

http://identifiers.org/hco/5/GRCh38#103168326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97661577-A-C

103168326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97661577-A-G

103168508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97661405-T-C

103168579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97661333-C-T

103168681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97661230-A-G

103168922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97661008-T-C

103169060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97660774-A-G

103169278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97660549-A-G

103169539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97660338-T-C

103169924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97660161-A-G

103170003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97660090-T-G

103171523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97659502-T-C

103171693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97659331-C-T

103171872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97659141-T-G

103171913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97659099-C-T

103172069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97658835-C-T

103172094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97658810-T-C

http://identifiers.org/hco/5/GRCh38#103172129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97658776-A-C

103172914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97658000-C-T

103172949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97657967-A-G

103172987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97657929-T-C

103173404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97657520-T-A

103173554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97657179-G-A

103173620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97657128-C-T

103173757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97656856-A-G

103173757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97656856-A-T

103176760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97655802-T-C

103176760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97655802-T-G

103176769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97655779-T-C

103176775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97655773-T-C

103176776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97655772-T-C

103176821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97655734-T-C

103176885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97655669-A-G

103176887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97655667-G-A

103176887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97655667-G-T

103176903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97655654-A-G

103176916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97655641-A-G

http://identifiers.org/hco/5/GRCh38#103176946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97655611-C-A

103177039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97655540-T-C

103177145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97655436-T-C

103177554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97655335-G-A

103177554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97655335-G-C

103177560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97655329-A-G

103177780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97655113-C-G

103177851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97655041-T-C

http://identifiers.org/hco/5/GRCh38#103178000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97654897-C-A

103179846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97651846-A-G

http://identifiers.org/hco/5/GRCh38#103179929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97651724-C-A

103180003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97651575-T-C

http://identifiers.org/hco/5/GRCh38#103180153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97651428-C-A

103180159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97651422-C-G

http://identifiers.org/hco/5/GRCh38#103180195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97651386-A-C

103180195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97651386-A-G

103180195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97651386-A-T

103180286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97651298-A-G

103180597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97651172-C-G

103180642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97651130-G-A

103181192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97650573-C-T

103181760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97650383-T-C

103181760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97650383-T-G

103181868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97650324-T-G

103181884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97650308-C-T

103182226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97649972-C-T

103182731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97649461-G-T

103182857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97649344-A-T

103183049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97649171-G-T

103183509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97648727-A-G

103183662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97648587-T-G

103183795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97648449-A-G

http://identifiers.org/hco/5/GRCh38#103183954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97648291-A-C

103184125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97648161-A-G

103184251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97648039-G-A

103184251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97648039-G-T

http://identifiers.org/hco/5/GRCh38#103184511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97647788-A-C

103184511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97647788-A-G

http://identifiers.org/hco/5/GRCh38#103184800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97647503-A-C

103184846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97647454-T-A

103184846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97647454-T-C

103185331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97646292-A-G

103185683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97645952-G-T

http://identifiers.org/hco/5/GRCh38#103186104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97645497-C-A

103186492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97645112-A-G

http://identifiers.org/hco/5/GRCh38#103186562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97645036-C-A

103186562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97645036-C-T

103186578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97645020-G-A

103186578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97645020-G-C

103186995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97644629-C-G

103187360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97644281-T-G

103187917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97643754-G-A

103187917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97643754-G-C

103188135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97643513-T-C

103188277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97643287-A-G

103188554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97643140-G-T

http://identifiers.org/hco/5/GRCh38#103188569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97643123-A-C

103188653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97643039-A-T

http://identifiers.org/hco/5/GRCh38#103188703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97642974-C-A

103188872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97642782-T-A

103188981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97642673-T-A

http://identifiers.org/hco/5/GRCh38#103189083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97642574-C-A

103189083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97642574-C-G

103189083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97642574-C-T

103189105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97642551-G-A

103189105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97642551-G-T

103189190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97642469-T-C

103189193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97642466-T-G

http://identifiers.org/hco/5/GRCh38#103189248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97642413-A-C

103189248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97642413-A-G

http://identifiers.org/hco/5/GRCh38#103189277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97642384-C-A

http://identifiers.org/hco/5/GRCh38#103189286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97642375-C-A

103189286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97642375-C-T

103189362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97642304-A-G

103189973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97641731-C-T

103189980-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97641724-T-A

103190771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97640936-C-T

http://identifiers.org/hco/5/GRCh38#103191031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97640683-A-C

103191031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97640683-A-G

103191112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97640599-G-A

103191112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron variant
orthologous variants: 97640599-G-T

http://identifiers.org/hco/5/GRCh38#103195138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97639351-C-A

103195138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97639351-C-T

103195163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97639328-C-T

103195239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97639235-A-G

103195609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97638942-A-T

103195614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97638937-C-T

103195628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97638927-C-T

103195662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97638892-C-G

103195672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97638882-C-T

103195698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97638856-A-G

103196308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97638311-C-T

103196527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97638143-C-T

103196768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97637912-G-A

103199479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97637163-A-T

103199517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97637129-T-C

103199566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97637083-G-A

103199566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97637083-G-C

103200079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97636590-T-C

103200803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97636196-T-G

103200911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97636131-T-C

103201114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97635933-A-G

103201197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97635850-A-G

103201259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97635799-A-G

103201372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97635692-A-G

103201399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97635668-T-C

103201400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97635667-A-G

http://identifiers.org/hco/5/GRCh38#103201441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97635629-C-A

103201441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97635629-C-G

103201450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97635620-G-A

103201453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97635617-T-G

103201460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97635610-A-G

103201650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 97635426-T-C

http://identifiers.org/hco/5/GRCh38#103201653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97635423-A-C

103201653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 97635423-A-G

103201666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 97635410-T-C

103201743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97635271-T-C

http://identifiers.org/hco/5/GRCh38#103201757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97635257-C-A

103201757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97635257-C-T

http://identifiers.org/hco/5/GRCh38#103201768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97635246-C-A

http://identifiers.org/hco/5/GRCh38#103201795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97635220-A-C

103201997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97635053-T-C

103202107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97634952-A-G

103202159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97634903-G-T

http://identifiers.org/hco/5/GRCh38#103202466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97634582-C-A

103202892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97634198-A-G

103202897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97634193-T-C

103202934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97634158-A-T

103202946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97634146-T-C

103202968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97634124-C-T

103202999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97634090-C-T

103203091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97633996-G-C

103203103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97633984-T-C

http://identifiers.org/hco/5/GRCh38#103203847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97633231-C-A

103203847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97633231-C-T

103203903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97633166-G-T

103204837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97631230-T-A

103204837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97631230-T-C

103205966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97630874-T-G

103206134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97630714-A-G

103206171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97630680-G-A

103206171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97630680-G-T

103206252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97630600-G-A

103206316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97630537-G-A

103206433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97630432-G-T

103206535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97630358-G-A

103206535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97630358-G-T

103206826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97630156-T-A

103207049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97630049-T-C

103207086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97630020-G-A

103207086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97630020-G-T

103207095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97630011-G-A

103207110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97629999-T-C

103207260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97629862-A-G

103207508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97629560-A-G

103207571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97629467-A-T

103207581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97629457-T-C

103207654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97629342-C-T

103207766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97629233-T-G

103207771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97629228-A-G

103207771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97629228-A-T

103207804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97629195-G-T

103207884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97629111-T-A

http://identifiers.org/hco/5/GRCh38#103207885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97629110-C-A

http://identifiers.org/hco/5/GRCh38#103208626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97627949-C-A

103208676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97627906-T-C

103209015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97627633-G-A

103209015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97627633-G-T

http://identifiers.org/hco/5/GRCh38#103209016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97627632-C-A

103209605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97626195-G-T

103209631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97626144-T-A

http://identifiers.org/hco/5/GRCh38#103209632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97626143-A-C

103209632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97626143-A-T

103209870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97625909-G-C

103209874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97625905-A-G

103209890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97625889-T-C

103209918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97625859-A-T

103210399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97625508-A-G

http://identifiers.org/hco/5/GRCh38#103210427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97625481-C-A

103210460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97625448-T-C

http://identifiers.org/hco/5/GRCh38#103210710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#97625160-C-A

103210920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97625005-T-C

103210982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97624943-G-A

103211001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29035
most severe consequence: 3 prime UTR variant
orthologous variants: 97624926-A-G