http://identifiers.org/hco/8/GRCh38#22367349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70588797-C-A

22367349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5 prime UTR variant
orthologous variants: 70588797-C-T

22367483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, undefined
orthologous variants: 70588661-G-A

22367483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, undefined
orthologous variants: 70588661-G-T

22367486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, undefined
orthologous variants: 70588658-G-T

22367547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 70588597-G-T

22367670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70588474-G-A

http://identifiers.org/hco/8/GRCh38#22367747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70588398-C-A

22367747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70588398-C-T

22367815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70588328-T-C

22367835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70588303-G-A

22367835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70588303-G-C

22367835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70588303-G-T

22368106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70588004-G-A

22368106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70588004-G-C

22368106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70588004-G-T

22368131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70587980-G-T

22368206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70587902-T-C

22368252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70587858-C-T

22368320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70587797-C-G

22369865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70586795-G-A

22369903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70586757-T-G

22369960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70586703-C-G

22369960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70586703-C-T

22369961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70586702-G-A

22369961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70586702-G-T

22370033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70586629-A-G

http://identifiers.org/hco/8/GRCh38#22370120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70586554-C-A

22370203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70586508-A-G

22370510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70586318-C-T

22370683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70586155-A-G

22370828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70586018-C-G

22370828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70586018-C-T

22370941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70585903-C-G

22371157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70585751-A-G

22371157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70585751-A-T

22371158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70585750-A-G

22372289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70584511-C-T

http://identifiers.org/hco/8/GRCh38#22372431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70584369-C-A

22372460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70584335-C-T

22372604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70584143-T-C

22372651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70584104-C-T

22378508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70579331-G-A

22378656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70578976-C-G

22378677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70578948-G-A

22378677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70578948-G-C

http://identifiers.org/hco/8/GRCh38#22378855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70578807-C-A

22378855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70578807-C-T

22378981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70578695-C-T

22379395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70578131-G-A

http://identifiers.org/hco/8/GRCh38#22379468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70578047-C-A

22379492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70578015-G-T

http://identifiers.org/hco/8/GRCh38#22379511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70577996-C-A

http://identifiers.org/hco/8/GRCh38#22383764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70574332-C-A

22384033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70574039-G-A

22384088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70573999-C-T

22384293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70573783-C-T

22387432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70572200-G-A

http://identifiers.org/hco/8/GRCh38#22388121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70571699-A-C

22388251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70571565-T-C

22388367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70571459-G-T

22388381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70571445-G-A

22388449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70571413-G-A

22388546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70571366-T-C

22389024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70570953-A-G

22389482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70570601-C-T

22389490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70570593-C-T

22391091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70568843-G-T

22392104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70567906-A-G

22392176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70567844-G-C

22392176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70567844-G-T

22392251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70567801-G-A

22392560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70567672-A-G

22392725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70567519-A-G

22392748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70567500-G-A

22392748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70567500-G-C

22392748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70567500-G-T

http://identifiers.org/hco/8/GRCh38#22393078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70567179-A-C

http://identifiers.org/hco/8/GRCh38#22393082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70567175-C-A

22393082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70567175-C-T

22393120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70567142-G-A

22393120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70567142-G-T

22393301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70566989-G-A

22393310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70566980-A-G

22393449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70566824-T-C

22396029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70562396-T-C

22396052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70562372-T-C

22396073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70562351-G-A

http://identifiers.org/hco/8/GRCh38#22398750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70561497-A-C

22398798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, splice_donor_variant
orthologous variants: 70561454-G-A

22398798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, splice_donor_variant
orthologous variants: 70561454-G-T

22398871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70561386-G-T

22398932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70561347-G-C

22398932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70561347-G-T

22399011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70561272-C-T

22399146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70561075-G-T

22399194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70561027-G-A

22399208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70561006-T-G

22399234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70560967-C-G

22399234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70560967-C-T

22399248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70560953-C-T

22399256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70560945-G-A

22399622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70560499-C-T

22399625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70560496-G-A

22399717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70560412-A-G

22399735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70560394-C-T

http://identifiers.org/hco/8/GRCh38#22399744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70560385-C-A

22399927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70560199-A-T

22400368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70559783-C-T

22400374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70559777-A-G

22400383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70559768-G-A

22400970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70558371-T-C

22401181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70558164-A-G

22401330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70558031-G-A

22401686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70557707-T-C

22401866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70557515-A-T

22404581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70556548-G-C

22404581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70556548-G-T

22404583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70556546-G-A

22404583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70556546-G-T

http://identifiers.org/hco/8/GRCh38#22404605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70556511-C-A

22404605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70556511-C-T

22404606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70556510-T-A

22404606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70556510-T-C

22404622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70556494-G-A

22404622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70556494-G-T

22404624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70556492-G-T

22404627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70556489-G-A

22404627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70556489-G-T

22404906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: missense variant
orthologous variants: 70556183-C-T

http://identifiers.org/hco/8/GRCh38#22405013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70556090-C-A

http://identifiers.org/hco/8/GRCh38#22405017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70556086-C-A

22405017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70556086-C-G

22405017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70556086-C-T

22405048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70556085-A-G

22405060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70556073-G-A

22405060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70556073-G-C

http://identifiers.org/hco/8/GRCh38#22405094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70556045-C-A

22405094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70556045-C-G

22405094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70556045-C-T

22405101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70556038-G-A

22405101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70556038-G-C

22405101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70556038-G-T

http://identifiers.org/hco/8/GRCh38#22405598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70555884-A-C

22405668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70555840-C-G

22405668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70555840-C-T

22405670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70555838-C-G

22405677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70555831-G-A

http://identifiers.org/hco/8/GRCh38#22405936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70555565-A-C

22405950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70555540-A-G

22405951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70555539-G-A

22405976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70555514-A-G

22408054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70554331-G-A

22408153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70554235-G-A

22408153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70554235-G-C

22408153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70554235-G-T

22408198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70554193-G-A

22408198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70554193-G-T

22408217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70554174-T-G

22408337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: missense variant
orthologous variants: 70554044-G-A

22408368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: missense variant
orthologous variants: 70554013-G-A

22409747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70553444-C-T

22409753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70553438-T-C

22409794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70553403-G-A

22409794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70553403-G-T

http://identifiers.org/hco/8/GRCh38#22409814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70553383-A-C

http://identifiers.org/hco/8/GRCh38#22410221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70553004-C-A

22410254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70552972-A-G

22410254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70552972-A-T

22410343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70552884-C-G

22410854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70552322-G-C

22410947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70552237-G-C

22411398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70551807-G-C

22411510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70551718-G-A

22411589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70551639-C-T

22411651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70551589-G-A

22411668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70551572-C-T

22411730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70551505-G-A

22411732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70551503-G-A

22411732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70551503-G-T

http://identifiers.org/hco/8/GRCh38#22411745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70551492-A-C

http://identifiers.org/hco/8/GRCh38#22411860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70551373-C-A

22411860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70551373-C-T

22411868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70551365-T-A

http://identifiers.org/hco/8/GRCh38#22411876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70551323-C-A

http://identifiers.org/hco/8/GRCh38#22411921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70551277-C-A

22411921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70551277-C-G

22411921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70551277-C-T

22411953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70551262-C-T

22412648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70550680-T-G

22412665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70550665-C-T

22412773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70550606-G-A

22412773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70550606-G-T

http://identifiers.org/hco/8/GRCh38#22412853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70550536-A-C

22412854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70550535-C-T

22412886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70550508-C-T

22413375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70550061-A-G

22413843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70549756-C-T

22414637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70548537-G-A

22414637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70548537-G-T

22414717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70548475-G-A

22414724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70548473-A-G

22414724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70548473-A-T

22414976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70548229-G-A

22414976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70548229-G-C

22415206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70548150-G-A

22415264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70548114-G-C

http://identifiers.org/hco/8/GRCh38#22415284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70548097-C-A

22415284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70548097-C-T

http://identifiers.org/hco/8/GRCh38#22415373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70548016-C-A

22415393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70547996-T-A

22415393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70547996-T-C

http://identifiers.org/hco/8/GRCh38#22415524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70547917-C-A

22415524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70547917-C-T

22415526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70547915-G-A

22415526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70547915-G-T

22415546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70547902-T-G

22415548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70547900-G-A

22415548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70547900-G-T

http://identifiers.org/hco/8/GRCh38#22415590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70547861-C-A

22415590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70547861-C-G

22415630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70547831-G-T

22415686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70547788-G-T

22415775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70547712-C-T

22416019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70547456-G-A

22416115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70547370-G-C

22416371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70547172-T-C

22416371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70547172-T-G

22416383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70547160-T-C

http://identifiers.org/hco/8/GRCh38#22416423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70547149-C-A

22416423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70547149-C-T

http://identifiers.org/hco/8/GRCh38#22416428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70547144-A-C

22416428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70547144-A-T

22416828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70546974-C-T

22417194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70546648-T-A

22417268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70546573-G-A

22417268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70546573-G-C

22417623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70546308-C-T

22417635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70546293-A-G

22417761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: missense variant
orthologous variants: 70546171-G-A

22417866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70546058-G-T

22419542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70544269-T-G

22419739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70544068-G-A

22419752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70544052-C-T

22420093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70543720-A-G

22420106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70543708-T-C

22420360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70543445-A-G

22420380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70543426-T-C

22420511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70543335-A-G

http://identifiers.org/hco/8/GRCh38#22420536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70543311-C-A

22420536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70543311-C-G

22420536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70543311-C-T

22420588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70543258-C-G

22420623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70543223-T-C

22420630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70543217-G-T

22420671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70543178-G-C

22420671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70543178-G-T

22420840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70543028-G-A

22420870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70543003-A-G

22420877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70542995-C-G

22420877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70542995-C-T

22420933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70542930-G-T

22420984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70542868-A-G

22421317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70542399-A-G

22421354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70542360-G-A

22421354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70542360-G-T

22421428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70542302-G-A

22421428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70542302-G-T

22421480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70542248-A-G

22421506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70542223-G-T

22421769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70541695-G-A

22421769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70541695-G-C

22421769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70541695-G-T

22422148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70541381-G-T

http://identifiers.org/hco/8/GRCh38#22422363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70541190-C-A

22422363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70541190-C-T

22422549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70541042-G-T

22422750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, undefined
orthologous variants: 70540614-T-C

22422752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, undefined
orthologous variants: 70540612-G-A

22422752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron_variant, undefined
orthologous variants: 70540612-G-C

http://identifiers.org/hco/8/GRCh38#22424558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70538154-C-A

22424674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70538030-A-T

22425633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70536852-A-G

22425654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70536831-T-C

22425684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70536790-T-C

http://identifiers.org/hco/8/GRCh38#22425856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70536642-A-C

http://identifiers.org/hco/8/GRCh38#22426515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70536596-C-A

22426515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70536596-C-T

22426640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70536487-C-G

22426685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70536447-T-C

22427514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70536135-A-G

22427514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70536135-A-T

22427515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70536134-A-G

http://identifiers.org/hco/8/GRCh38#22427524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70536125-A-C

22427599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20858
most severe consequence: intron variant
orthologous variants: 70536060-T-G