18155351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47196977-T-A

18155351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47196977-T-C

18155397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 5 prime UTR variant
orthologous variants: 47197005-G-T

18155419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, undefined
orthologous variants: 47197027-G-A

18155419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, undefined
orthologous variants: 47197027-G-C

18155419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, undefined
orthologous variants: 47197027-G-T

18155513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47197103-G-C

18155513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47197103-G-T

18155932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, undefined
orthologous variants: 47197699-C-T

18155967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, undefined
orthologous variants: 47197730-T-C

18156079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47197866-C-T

18156318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47198212-T-C

18156975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47198861-A-T

18157159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47199153-A-G

18157226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47199293-G-A

18157323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47199392-C-T

18157324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47199393-G-A

18157324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47199393-G-T

18157510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47199550-G-T

18157725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47199714-A-G

18158500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47200461-C-T

18159866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47201353-T-C

18159870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47201357-T-A

18160044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47201513-T-C

http://identifiers.org/hco/6/GRCh38#18160076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47201540-C-A

18160076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47201540-C-T

18160078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47201542-T-C

18160420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47201813-A-G

18161187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47202431-G-A

http://identifiers.org/hco/6/GRCh38#18161245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47202569-C-A

18161245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47202569-C-G

18161246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47202570-T-C

18161312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47202639-C-T

18161361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, missense_variant
orthologous variants: 47202688-A-G

18161361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, missense_variant
orthologous variants: 47202688-A-T

18161507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47202834-T-C

18161558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47202884-T-C

18161562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47202887-A-G

http://identifiers.org/hco/6/GRCh38#18161573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47202898-C-A

18161573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47202898-C-G

18161573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47202898-C-T

18161747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47203018-A-G

18161834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47203092-A-G

http://identifiers.org/hco/6/GRCh38#18161839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47203097-A-C

18161839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47203097-A-G

http://identifiers.org/hco/6/GRCh38#18161843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47203101-C-A

18161844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47203102-A-G

18162321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47203440-C-T

18162398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47203517-T-C

18162440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47203558-T-G

http://identifiers.org/hco/6/GRCh38#18162710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47203980-C-A

18162711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47203981-T-C

18162727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47203998-A-G

http://identifiers.org/hco/6/GRCh38#18162800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47204056-C-A

18162800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47204056-C-T

18162801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47204057-A-G

http://identifiers.org/hco/6/GRCh38#18162850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47204101-C-A

18162961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47204204-G-C

18162964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47204207-G-A

18166401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47205392-T-A

http://identifiers.org/hco/6/GRCh38#18166422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47205407-C-A

18171322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47207054-T-G

18171329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47207061-A-G

18171404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 47207136-T-C

18171485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47207217-T-C

18171501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47207236-G-T

http://identifiers.org/hco/6/GRCh38#18171611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47207326-C-A

18171611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47207326-C-G

18171797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47207469-A-G

18171838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47207505-G-A

18171877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47207540-G-C

http://identifiers.org/hco/6/GRCh38#18171946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47207590-A-C

18171950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47207594-G-A

18172178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47207754-A-G

18172178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47207754-A-T

18172377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47207901-T-A

18172377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47207901-T-C

18184977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47211488-G-A

18185240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47211806-T-A

18185537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47211992-G-C

18185585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47212035-G-A

18185631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47212079-T-A

18185631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47212079-T-C

18185801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 47212281-A-G

18186035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47212507-A-T

18186112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47212581-G-A

18187505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47213993-C-T

18187561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47214043-A-T

18187606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47214088-T-A

18187606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47214088-T-C

http://identifiers.org/hco/6/GRCh38#18187671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47214145-A-C

18187671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47214145-A-T

18188012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47214467-A-G

http://identifiers.org/hco/6/GRCh38#18188015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47214469-C-A

18188015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47214469-C-T

http://identifiers.org/hco/6/GRCh38#18188040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47214493-C-A

18188271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47214825-A-T

18188395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47215017-A-G

18188434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47215062-G-A

18191360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 47216597-A-G

18191396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47216633-G-T

http://identifiers.org/hco/6/GRCh38#18191410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47216652-C-A

18191410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47216652-C-T

18197049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 47217522-A-G

http://identifiers.org/hco/6/GRCh38#18197052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47217525-C-A

18197052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 47217525-C-T

18197182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 47217655-A-G

http://identifiers.org/hco/6/GRCh38#18197273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47217744-C-A

18197285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47217757-T-C

18197343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47217804-G-T

18197541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47218007-T-C

18197643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 47218103-G-A

http://identifiers.org/hco/6/GRCh38#18197743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47218204-C-A

18197743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47218204-C-G

18197743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47218204-C-T

18198807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47219666-G-C

18198807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47219666-G-T

18200126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47220629-G-A

18200126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47220629-G-T

http://identifiers.org/hco/6/GRCh38#18200463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47220945-A-C

18200672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47221230-A-G

http://identifiers.org/hco/6/GRCh38#18200813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47221356-A-C

18201064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47221584-T-C

18201226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47221722-G-A

http://identifiers.org/hco/6/GRCh38#18201378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47221835-A-C

http://identifiers.org/hco/6/GRCh38#18201397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47221847-A-C

18201397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47221847-A-G

18201919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47222390-T-G

18202457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47222632-A-G

18202538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47222701-G-C

18202553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47222716-A-G

18202612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47222774-G-T

18202643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47222802-C-T

18203461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47223794-C-T

18203529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47223859-A-G

18204521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47224421-T-C

18204762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47224714-C-G

18204762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47224714-C-T

18205205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47225096-T-C

http://identifiers.org/hco/6/GRCh38#18205230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47225115-C-A

18205258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47225143-G-A

18205258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47225143-G-T

http://identifiers.org/hco/6/GRCh38#18205423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47225265-A-C

18205423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47225265-A-G

18205477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47225305-A-G

18205484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47225312-T-C

18205484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47225312-T-G

18205485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47225313-G-T

18205519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47225350-G-A

18205519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47225350-G-T

18205715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47225505-C-T

18205727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47225519-C-T

18205771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47225559-A-G

18205771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47225559-A-T

18205801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47225578-G-A

18205801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47225578-G-T

18205810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47225587-G-A

18205810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47225587-G-T

18205862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47225640-C-T

18206017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47225838-G-A

http://identifiers.org/hco/6/GRCh38#18206758-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47226438-A-C

18206772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47226455-C-T

18206805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47226488-C-T

18206853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47226526-C-T

http://identifiers.org/hco/6/GRCh38#18206913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47226578-A-C

18207047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47226694-G-A

18207120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47226778-A-G

18207157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47226815-A-G

18207234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47226982-T-C

18207253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47227007-A-G

18207314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47227103-C-T

18207332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47227121-T-C

18207332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47227121-T-G

18207333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47227122-A-G

18207348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47227136-C-T

18207364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47227151-C-T

18207505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 47227294-G-A

18207505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 47227294-G-T

18207570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47227354-G-C

18207663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47227462-A-G

18207663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47227462-A-T

18207726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47227525-T-C

18207854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47227612-T-C

18207925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47227649-C-T

http://identifiers.org/hco/6/GRCh38#18208028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47227735-C-A

18208028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47227735-C-T

http://identifiers.org/hco/6/GRCh38#18208241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47227935-C-A

18208241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47227935-C-G

18208241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47227935-C-T

18208370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47228060-G-A

18208407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47228093-C-T

18208890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47228204-A-G

18208902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47228214-C-T

18208982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47228290-A-G

18208997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47228305-G-A

18209349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47228666-C-T

18209928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47228963-G-C

18210004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47229038-T-C

18210147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47229166-T-C

18210289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47229307-A-T

18211297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47229615-C-G

18211297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron variant
orthologous variants: 47229615-C-T

18211504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47229814-G-A

http://identifiers.org/hco/6/GRCh38#18211518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47229828-C-A

18211518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47229828-C-T

18211566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47229859-A-G

18212096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47230401-C-T

18212213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47230517-G-T

18212214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47230518-G-A

18212214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47230518-G-T

18212222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47230526-G-T

18212327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47230670-T-G

http://identifiers.org/hco/6/GRCh38#18212345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47230682-C-A

18212345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47230682-C-T

18212412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47230776-G-A

18212412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47230776-G-T

http://identifiers.org/hco/6/GRCh38#18212483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47230854-C-A

18212483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 47230854-C-T

http://identifiers.org/hco/6/GRCh38#18212624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47230997-C-A

18212624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47230997-C-T

18213748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47231836-G-A

18214061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232103-A-G

18214513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232482-C-T

18214904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232623-T-A

18214904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232623-T-C

18214905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232624-G-T

http://identifiers.org/hco/6/GRCh38#18215196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47232781-C-A

18215203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232788-G-T

18215258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232846-T-C

18215321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232894-C-T

18215587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233082-G-A

http://identifiers.org/hco/6/GRCh38#18215724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47233167-A-C

18215724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233167-A-T

18215741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47233183-C-T

18217840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47234019-T-G

18217867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47234046-C-G

18217867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47234046-C-T

18218190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47234284-A-T

18218450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47234467-A-G

18221837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47236285-T-C

18221855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47236292-T-A

18221855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47236292-T-C

18221893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47236335-T-C

18222038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47236479-T-A

18222038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47236479-T-C

18222125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47236561-A-G

18222154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47236590-A-G

18222155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47236591-G-C

18222155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47236591-G-T

http://identifiers.org/hco/6/GRCh38#18222250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47236672-A-C

18222250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47236672-A-T

18222275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47236683-G-C

18222278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47236686-T-G

18222339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47236744-T-G

http://identifiers.org/hco/6/GRCh38#18222340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47236745-C-A

18222555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47236940-G-T

18222761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47237116-T-A

http://identifiers.org/hco/6/GRCh38#18222804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47237138-A-C

http://identifiers.org/hco/6/GRCh38#18222816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47237150-C-A

18222816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47237150-C-T

18222969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47237285-T-C

18223004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47237319-C-T

18223441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21577
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47237704-G-A