112149916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55056120-G-T

112149966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55056173-G-T

112149967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55056174-C-T

112150133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55056338-T-C

112150133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55056338-T-G

112150143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55056347-A-G

112150382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55056606-T-A

112150382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55056606-T-C

112150477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55056685-T-C

112150595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55056793-C-G

112150595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55056793-C-T

112150712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55056892-G-T

112150922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55057052-T-C

112150929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55057058-A-G

112151003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55057121-C-T

112151296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55057411-T-C

112151587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55057658-A-G

112151603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55057674-G-T

112151609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55057680-T-A

112151709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55057766-G-T

112151713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55057770-G-A

112151716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55057773-T-A

112151716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55057773-T-C

112151791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55057862-C-G

112151873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55057938-A-G

112152022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55058071-T-A

http://identifiers.org/hco/10/GRCh38#112152044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55058093-C-A

112152044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55058093-C-T

112152045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55058094-A-G

112152083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55058130-G-T

112152197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55058240-A-G

112152305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55058340-T-C

112152459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55058456-T-C

112152601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55058598-C-T

112152606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55058603-T-C

112152849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55058772-G-A

112152849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55058772-G-T

112152942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55058860-C-G

112153091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55058973-G-T

112153092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55058974-G-A

112153092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55058974-G-T

112153105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55058987-T-C

112153115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55058996-A-G

112153324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55059153-A-G

112153465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55059283-G-A

112153465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55059283-G-C

112153465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55059283-G-T

112153497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55059312-C-G

112153497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3 prime UTR variant
orthologous variants: 55059312-C-T

http://identifiers.org/hco/10/GRCh38#112153749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55059562-C-A

112153792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55059599-G-A

112153792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55059599-G-C

112153792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55059599-G-T

112153819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55059628-G-A

112153819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55059628-G-T

112153821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55059630-G-A

112153821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55059630-G-T

http://identifiers.org/hco/10/GRCh38#112153826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55059644-C-A

112153826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55059644-C-G

112153826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55059644-C-T

112153837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55059656-A-G

112153837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55059656-A-T

112153838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55059657-G-A

112153838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55059657-G-T

112153840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55059659-T-G

http://identifiers.org/hco/10/GRCh38#112153843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55059660-C-A

112153843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55059660-C-T

112154462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55060988-A-G

http://identifiers.org/hco/10/GRCh38#112154475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55061002-C-A

112154497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55061019-T-C

112154534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55061056-G-A

112154534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55061056-G-T

112154538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55061060-T-C

112154851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55061332-G-T

112155041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55061492-T-C

112155041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55061492-T-G

http://identifiers.org/hco/10/GRCh38#112155060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55061504-A-C

112155060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55061504-A-G

http://identifiers.org/hco/10/GRCh38#112155064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55061508-A-C

112155064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55061508-A-T

http://identifiers.org/hco/10/GRCh38#112155141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55061594-C-A

112155167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55061614-A-G

http://identifiers.org/hco/10/GRCh38#112155214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55061672-C-A

112155504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55061930-T-A

112155533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55061959-A-G

http://identifiers.org/hco/10/GRCh38#112155608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55062045-C-A

http://identifiers.org/hco/10/GRCh38#112155679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55062106-C-A

112155679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55062106-C-T

112155765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55062179-G-A

112155765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55062179-G-T

http://identifiers.org/hco/10/GRCh38#112155830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55062241-A-C

112155830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55062241-A-G

112155830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55062241-A-T

112155841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55062978-G-A

112155841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55062978-G-C

112155841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55062978-G-T

112155853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55062992-A-G

112155871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 55063010-T-C

112155907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 55063046-G-T

112155946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 55063085-A-G

112156113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063246-T-A

112156113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063246-T-C

112156138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063267-C-T

http://identifiers.org/hco/10/GRCh38#112156139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55063268-C-A

112156140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063269-A-G

112156141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063270-G-A

112156290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063407-G-T

http://identifiers.org/hco/10/GRCh38#112156293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55063410-C-A

112156313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063430-G-C

112156313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063430-G-T

112156396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063513-T-C

http://identifiers.org/hco/10/GRCh38#112156408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55063525-C-A

112156408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063525-C-T

http://identifiers.org/hco/10/GRCh38#112156423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55063540-A-C

112156993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063719-T-A

112157042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063767-G-T

112157072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063793-T-A

112157096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063818-A-G

112157143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063871-G-A

112157143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063871-G-T

http://identifiers.org/hco/10/GRCh38#112157164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55063896-C-A

112157180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063910-G-A

112157180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063910-G-T

http://identifiers.org/hco/10/GRCh38#112157202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55063930-C-A

112157202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063930-C-T

112157205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063932-C-T

112157210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063937-T-A

112157210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063937-T-C

112157210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063937-T-G

112157211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55063938-A-T

112157291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: missense variant
orthologous variants: 55064016-T-A

112157325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: missense variant
orthologous variants: 55064047-T-C

112157397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 55064119-A-G

112157411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55064133-T-C

http://identifiers.org/hco/10/GRCh38#112157442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55064171-A-C

112157442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55064171-A-G

http://identifiers.org/hco/10/GRCh38#112157508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55064221-C-A

112157508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55064221-C-G

112157508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55064221-C-T

112157759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55064437-C-T

112157780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55064456-C-T

112158283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55064691-T-C

http://identifiers.org/hco/10/GRCh38#112158500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55064863-C-A

112158500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55064863-C-T

112158515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55064877-G-T

112158522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55064884-T-A

112158522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55064884-T-C

112158522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55064884-T-G

http://identifiers.org/hco/10/GRCh38#112158541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55064903-C-A

112158541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55064903-C-T

http://identifiers.org/hco/10/GRCh38#112158542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55064904-A-C

112158545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55064907-G-A

112158545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55064907-G-T

112158547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55064909-C-T

112158561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55064919-G-A

112158708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55065062-C-T

112158749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55065093-G-C

112158808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55065152-T-C

112158840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55065183-C-T

112159128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55065415-G-C

112159134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55065421-G-A

112159718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55066049-G-A

112159765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55066093-G-A

112159765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55066093-G-T

112159777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55066105-A-T

112159884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55066241-A-G

112159885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55066242-G-A

112160028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: 55066375-G-A

112160028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: missense variant
orthologous variants: 55066375-G-C

112160028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: missense variant
orthologous variants: 55066375-G-T

112160139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55066483-T-A

112160159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55066504-G-C

112160159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55066504-G-T

112160182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55066530-T-A

112160182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55066530-T-C

112160218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55066553-G-A

112160218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55066553-G-T

112160249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55066571-G-T

112160274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55066598-C-T

112160279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55066603-C-G

112160416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55066641-T-A

112160416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55066641-T-C

112160489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55066681-G-T

112160686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: 55066837-G-A

112160716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: 55066867-A-G

112160806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: 55066957-A-G

112160815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: 55066966-G-A

112160990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55067106-G-A

112160990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55067106-G-C

http://identifiers.org/hco/10/GRCh38#112161007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55067123-C-A

112161007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55067123-C-T

112161047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55067153-G-T

112161062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55067167-C-G

112161166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55067241-A-T

112161526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55067539-G-A

112161526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55067539-G-T

112161531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55067544-G-T

112161537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55067550-A-G

112161537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55067550-A-T

112161562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55067575-G-C

112161562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55067575-G-T

112161649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55067631-G-T

112161694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: 55067675-A-G

http://identifiers.org/hco/10/GRCh38#112161783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55067756-C-A

112161827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55067798-T-C

112162044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55068005-G-T

112162159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55068098-T-C

112162174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55068113-G-A

112162197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55068138-T-C

112162197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55068138-T-G

112163371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55068516-T-C

112163511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55068635-T-G

http://identifiers.org/hco/10/GRCh38#112163614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55068740-C-A

112163616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55068742-T-A

112163618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55068744-A-G

112163619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55068745-G-T

112163642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55068768-T-C

http://identifiers.org/hco/10/GRCh38#112163652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55068778-C-A

112163654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55068780-A-T

112163670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55068787-G-T

112163807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: 55068922-A-G

112163813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: 55068928-G-A

112163813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: 55068928-G-T

http://identifiers.org/hco/10/GRCh38#112163841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55068950-A-C

112163841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55068950-A-G

112163841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55068950-A-T

112163842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55068966-C-G

112163843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55068967-A-G

112163843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55068967-A-T

http://identifiers.org/hco/10/GRCh38#112163955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55069218-C-A

112164066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55069334-C-T

112164452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55069754-T-C

112164489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55069794-A-T

112164539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: 55069838-A-G

http://identifiers.org/hco/10/GRCh38#112164566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55069865-A-C

112164710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55069998-A-T

112166513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 55070145-G-A

112166513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 55070145-G-T

http://identifiers.org/hco/10/GRCh38#112167664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55071204-C-A

112167720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55071258-G-A

112167722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55071260-A-T

http://identifiers.org/hco/10/GRCh38#112167725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55071263-A-C

112167725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55071263-A-G

112167881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55071395-T-G

http://identifiers.org/hco/10/GRCh38#112168117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55071488-A-C

112168167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55071533-A-G

http://identifiers.org/hco/10/GRCh38#112168175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55071541-C-A

112168387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: 55071708-G-A

http://identifiers.org/hco/10/GRCh38#112168465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55071786-A-C

112168471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: 55071792-G-A

http://identifiers.org/hco/10/GRCh38#112168498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55071819-C-A

112168498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: 55071819-C-T

112168554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55071872-A-G

112168554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55071872-A-T

112168609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55071926-A-G

http://identifiers.org/hco/10/GRCh38#112168723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55072033-A-C

112168723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55072033-A-G

112168727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55072037-T-C

112168727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55072037-T-G

112168730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55072040-A-G

112168837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55072114-T-C

112168837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55072114-T-G

112169022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55072300-T-C

112169025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55072303-A-G

112169067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55072346-G-A

112169067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55072346-G-T

112169107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55072380-A-G

112169213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55072456-T-C

112169528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55073537-A-G

112169528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55073537-A-T

http://identifiers.org/hco/10/GRCh38#112170318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55073830-A-C

http://identifiers.org/hco/10/GRCh38#112170468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55073944-A-C

112170530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55074001-G-A

112170732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55074381-G-A

112170803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55074453-G-A

112170832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55074460-A-T

112171026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55074622-C-T

112171037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55074632-G-A

112171037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55074632-G-T

112171229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55074796-T-C

112171272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55074826-G-A

112171502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55075045-C-T

112171617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55075160-C-T

112171932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55075389-C-T

112172014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55075472-T-C

112172080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55075529-A-T

112172082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55075531-G-T

112172137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55075582-C-T

http://identifiers.org/hco/10/GRCh38#112172140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55075587-A-C

112172189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: missense variant
orthologous variants: 55075824-T-C

112172280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: 55075915-G-A

112172317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 55075952-G-A

112172337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55075971-C-T

112172390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55076015-G-T

112172561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55076164-T-C

112172611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55076224-G-T

112172639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55076232-A-T

112172661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55076244-C-T

http://identifiers.org/hco/10/GRCh38#112172685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55076254-A-C

112172685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55076254-A-T

112172874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55076415-T-G

http://identifiers.org/hco/10/GRCh38#112172926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55076485-C-A

112172926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55076485-C-T

112172973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: 55076546-A-G

112172973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: 55076546-A-T

112173030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: 55076603-G-A

112173030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: missense variant
orthologous variants: 55076603-G-T

112173087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55076659-A-G

112173111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55076681-G-A

112173111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55076681-G-T

112173151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55076705-A-G

112173216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55076769-G-A

112173240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55076798-T-A

112173489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55077041-T-C

112173499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55077051-G-C

112173543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55077090-T-C

112173601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55077145-G-T

112173785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: 55077316-C-T

112175194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55079181-G-A

112175285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55079257-T-C

112175285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55079257-T-G

112175363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55079348-T-C

112175392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55079377-C-T

112175486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55079457-A-G

112175495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55079466-G-C

http://identifiers.org/hco/10/GRCh38#112175497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55079468-C-A

http://identifiers.org/hco/10/GRCh38#112175573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55079539-C-A

112175573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55079539-C-T

112175680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: 55079648-G-A

112175680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: stop gained
orthologous variants: 55079648-G-C

112175716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 55079684-G-A

112175716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 55079684-G-T

112175718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 55079686-G-A

112175718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 55079686-G-T

http://identifiers.org/hco/10/GRCh38#112175891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55079845-C-A

112175920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55079874-G-A

112176417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55080304-T-C

http://identifiers.org/hco/10/GRCh38#112176636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55080511-A-C

112176738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55080591-A-G

112176906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55080789-T-C

112176906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55080789-T-G

112177739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55082130-G-A

http://identifiers.org/hco/10/GRCh38#112177837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55082210-C-A

112177837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55082210-C-T

112177857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55082230-T-C

112177930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55082297-A-G

112177939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55082306-T-C

112177939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55082306-T-G

112177992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: 55082359-A-G

112177992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: synonymous variant
orthologous variants: 55082359-A-T

112178125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55082490-G-C

112178161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55082532-G-A

112178161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55082532-G-T

http://identifiers.org/hco/10/GRCh38#112178178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55082549-C-A

112178178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55082549-C-T

112178199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55082575-A-T

112178205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55082581-A-G

112178609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55082647-G-A

112178731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55082787-G-A

112178765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55082812-A-G

112178805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55082853-G-C

112179026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55082983-G-C

http://identifiers.org/hco/10/GRCh38#112179042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55082999-A-C

112179252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55083183-C-T

112179274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55083199-T-C

112179277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55083202-C-T

http://identifiers.org/hco/10/GRCh38#112179451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55083794-A-C

112179784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55084111-T-C

112180344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55084435-G-T

112180434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron variant
orthologous variants: 55084529-A-T

112180512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: missense variant
orthologous variants: 55084592-A-T

112180609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55084689-A-G

112180609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55084689-A-T

http://identifiers.org/hco/10/GRCh38#112180616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55084696-A-C

112180625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55084702-T-G

112180696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55084761-T-A

112180696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55084761-T-C

112180698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55084791-G-T

http://identifiers.org/hco/10/GRCh38#112180699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55084792-C-A

112180699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55084792-C-G

112180711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55084804-G-T

http://identifiers.org/hco/10/GRCh38#112180734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55084829-C-A

112180734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55084829-C-T

http://identifiers.org/hco/10/GRCh38#112180743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55084838-C-A

112180812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55085041-G-A

http://identifiers.org/hco/10/GRCh38#112180847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55085115-A-C

112181071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55085365-A-G

http://identifiers.org/hco/10/GRCh38#112181160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55085446-C-A

112181160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55085446-C-T

112181180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55085466-T-A

112181180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55085466-T-C

112181272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55085536-C-T

112181352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55085621-T-C

112181386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55085653-C-T

112181477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55085739-A-G

112181659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55085905-T-C

112181673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55085919-C-T

112181799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 55086045-T-C

http://identifiers.org/hco/10/GRCh38#112181916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55086156-C-A

112182136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55086378-T-C

112182190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55086414-G-A

112182190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55086414-G-T

112182259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55086472-G-A

112182286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55086508-A-G

112182681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55086882-A-G

http://identifiers.org/hco/10/GRCh38#112182695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55086896-C-A

112182695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55086896-C-T

http://identifiers.org/hco/10/GRCh38#112182730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55086929-C-A

112182730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55086929-C-T

112182768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55086968-C-T

http://identifiers.org/hco/10/GRCh38#112182858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55087047-C-A

112182858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 55087047-C-T

112182881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 55087072-G-A

112182881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 55087072-G-T

http://identifiers.org/hco/10/GRCh38#112183024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55087246-C-A

112183024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55087246-C-T

http://identifiers.org/hco/10/GRCh38#112183026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55087248-C-A

112183026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55087248-C-G

112183026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55087248-C-T

112183232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55087452-T-C

112183356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55087550-C-T

112183395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55087595-C-T

112183400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55087598-T-C

112183647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55087777-G-T

http://identifiers.org/hco/10/GRCh38#112183652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55087781-A-C

112183652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55087781-A-G

112183681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55087815-G-A

112183681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55087815-G-T

112183718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55087865-G-A

112183718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55087865-G-T

112183723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55087870-A-G

112183737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55087882-G-C

112183737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55087882-G-T

112183766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55087907-A-G

http://identifiers.org/hco/10/GRCh38#112183809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#55087951-C-A

112183809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55087951-C-T

112183962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55088046-A-T

http://identifiers.org/hco/10/GRCh38#112184102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55088198-A-C

112188886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55090942-G-A

112189774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55091771-A-G

112191073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55092518-G-A

112191073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55092518-G-C

112192016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55092634-G-C

112192756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55094211-G-A

112192840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55094289-A-G

112193091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55094521-G-A

112193095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55094525-G-A

112193155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55094582-G-A

112193330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55094709-G-C

112193542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55094910-T-C

112193994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55096378-C-T

http://identifiers.org/hco/10/GRCh38#112194082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55096472-C-A

112194082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55096472-C-T

112194179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55096570-T-G

112194214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55096620-G-A

112194275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55096674-C-G

112194385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55096783-A-G

112194469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55096873-C-T

112194551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55096954-A-G

112194723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55097084-G-C

http://identifiers.org/hco/10/GRCh38#112194810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55097160-C-A

112194810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55097160-C-T

112194826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55097176-A-G

112195054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55097383-A-G

http://identifiers.org/hco/10/GRCh38#112195118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55097444-A-C

112195118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55097444-A-G

http://identifiers.org/hco/10/GRCh38#112195218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55097471-C-A

112195218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55097471-C-T

112195263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55097499-T-C

http://identifiers.org/hco/10/GRCh38#112195357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55097589-C-A

112195357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55097589-C-G

112195963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55098070-C-T

112196038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55098146-G-A

112196038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55098146-G-T

112196056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55098164-G-A

112196084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55098192-C-T

112196160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55098262-T-C

112196631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55098746-C-T

112196732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55098815-T-C

112196869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55098924-G-C

112196869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55098924-G-T

112197021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55099058-G-C

http://identifiers.org/hco/10/GRCh38#112200836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55102067-C-A

112201181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55102414-C-T

112201448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55102661-C-T

112201498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55102709-C-T

112201756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55102960-T-C

112201791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55102996-G-A

112201791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55102996-G-C

112201820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55103005-G-T

112201870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55103054-G-A

112202291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55103495-A-G

112202362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55103560-T-A

112202631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55104174-T-C

112202631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55104174-T-G

112202709-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55104235-T-A

112202775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55104292-T-C

http://identifiers.org/hco/10/GRCh38#112202831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55104348-C-A

112203108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55104600-G-A

112203159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55105422-C-T

112203380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55105623-T-A

112203380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55105623-T-C

112203407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55105650-T-G

112203746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55106355-C-T

112203759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55106368-G-C

112203793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55106406-C-T

112203794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55106407-T-G

http://identifiers.org/hco/10/GRCh38#112203945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55106518-A-C

112204158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55106741-T-C

112207787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55108485-C-G

http://identifiers.org/hco/10/GRCh38#112207856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55108550-C-A

112207856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55108550-C-T

112207891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55108579-T-C

112208095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55108765-G-T

112208107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55108777-C-T

112208331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55108950-G-A

112208331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55108950-G-T

112208439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55109050-G-A

112208599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55109203-T-C

112209215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55110543-A-G

112209290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55110615-C-G

112209303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55110628-C-T

112209385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55110688-G-T

112209561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55110839-C-T

http://identifiers.org/hco/10/GRCh38#112209583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55110852-C-A

112210034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55111343-A-G

112210143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55111438-A-T

112210461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55111767-C-T

112210483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55111790-T-G

112210806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55112094-G-A

112210806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55112094-G-C

112210834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55112111-G-A

http://identifiers.org/hco/10/GRCh38#112210840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55112117-A-C

112211131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55112384-A-G

112211155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55112404-T-C

112211158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55112407-G-C

112211339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55112536-A-G

112211357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55112560-T-C

112211639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55112810-A-G

112211770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55112924-C-T

112211837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55112981-G-T

112211912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55113058-C-T

112213567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55114078-G-A

112213702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55114207-G-A

112213753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55114253-G-T

http://identifiers.org/hco/10/GRCh38#112213772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55114271-A-C

112213772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55114271-A-G

112213856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55114353-T-C

112214068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55114552-C-T

http://identifiers.org/hco/10/GRCh38#112214125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55114605-A-C

112214202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55114671-A-G

http://identifiers.org/hco/10/GRCh38#112214227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55114694-C-A

112214241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55114703-A-G

112214265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55114708-T-C

http://identifiers.org/hco/10/GRCh38#112214389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55114805-C-A

http://identifiers.org/hco/10/GRCh38#112214406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55114822-C-A

112214433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55114826-G-T

112214548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55114896-C-G

112214612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55114949-C-T

112214613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55114950-G-A

112214889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55115194-G-A

112215027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55115329-T-G

112215030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55115332-T-C

112215099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55115381-G-A

http://identifiers.org/hco/10/GRCh38#112215109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55115389-C-A

112215109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55115389-C-T

112215110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55115390-G-A

112215119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55115399-G-T

112215187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55115462-G-A

112215217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55115490-T-C

112215217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55115490-T-G

http://identifiers.org/hco/10/GRCh38#112215254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55115531-C-A

112215259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55115535-T-C

112215306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55115575-G-A

112215306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55115575-G-T

112215314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55115583-G-T

112215335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55115604-C-T

http://identifiers.org/hco/10/GRCh38#112215337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55115606-C-A

112215337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55115606-C-T

112215358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55115627-C-T

http://identifiers.org/hco/10/GRCh38#112215360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55115629-C-A

112215360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24865
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55115629-C-T