84328609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5 prime UTR variant
orthologous variants: 36690696-C-G

84328609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5 prime UTR variant
orthologous variants: 36690696-C-T

http://identifiers.org/hco/10/GRCh38#84328676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36690629-C-A

84328676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5 prime UTR variant
orthologous variants: 36690629-C-T

84328718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 36690586-C-T

84328903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36690418-G-C

84328903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36690418-G-T

84328906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36690415-C-T

84329319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36690004-T-A

84329623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36689519-C-T

84329849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36689321-T-C

84329954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36689220-C-T

84329971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36689203-A-G

84330230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36689009-C-G

84330923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36688210-A-G

84331027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36688025-G-C

84331056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36687810-A-G

http://identifiers.org/hco/10/GRCh38#84331177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36687637-A-C

84331177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36687637-A-G

84331377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36687485-A-G

84331913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36687027-T-A

84332231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36686645-G-A

84332724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36686299-G-C

84332917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36686037-T-C

84332925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36686029-G-A

84332998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36685953-T-C

84333105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36685840-A-G

84333132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36685813-A-G

84333196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36685758-T-C

84333313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36685662-C-G

84333313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36685662-C-T

84333450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36685541-A-G

84333512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36685477-A-G

84333616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36685287-G-A

84333671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36685232-G-C

84334435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36684502-C-T

84334447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36684490-G-T

http://identifiers.org/hco/10/GRCh38#84336224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36683444-C-A

84336267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36683403-G-A

84336443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36683234-A-G

84336459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36683218-G-C

84336818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36682536-G-T

84337079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36682293-T-C

84337279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36681961-C-T

84337280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36681960-T-A

http://identifiers.org/hco/10/GRCh38#84337293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#36681947-C-A

84337378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, undefined
orthologous variants: 36681832-G-A

84337394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, undefined
orthologous variants: 36681816-G-A

84337628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36681621-A-G

84337645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36681603-G-A

84340480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36680478-C-T

84340939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36679978-T-C

84341606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36679861-C-T

http://identifiers.org/hco/10/GRCh38#84341659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#36679809-A-C

84341745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36679719-G-A

84341765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36679699-T-C

http://identifiers.org/hco/10/GRCh38#84341902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36679629-A-C

84341913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36679618-C-G

84342015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36679507-T-G

http://identifiers.org/hco/10/GRCh38#84342180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36679373-C-A

84342340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36679226-C-T

84342384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36679182-A-G

84342523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36679073-G-A

84342523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36679073-G-C

84342769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36678860-T-C

84343584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36678435-G-T

84343641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36678379-A-G

http://identifiers.org/hco/10/GRCh38#84343965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36677670-A-C

84343965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36677670-A-G

http://identifiers.org/hco/10/GRCh38#84344066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36677593-C-A

84344083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36677573-A-G

http://identifiers.org/hco/10/GRCh38#84344200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36677469-A-C

84344200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36677469-A-G

84344378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36677189-C-T

84344537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36677079-A-G

84344653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36676969-C-T

84344670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36676952-G-A

84344722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36676895-C-T

84344723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36676894-A-T

84345218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36675894-C-T

http://identifiers.org/hco/10/GRCh38#84345281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36675829-C-A

84345343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36675772-C-T

84352423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36674292-C-G

84353172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36671826-T-C

84353176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36671822-A-G

84353268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36671737-G-T

84353292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36671713-A-G

84353411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36671596-G-T

84353432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36671568-A-G

84353561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36671446-C-T

84353608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36671401-A-G

84353608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36671401-A-T

84353740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36671253-T-C

http://identifiers.org/hco/10/GRCh38#84357915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36668114-A-C

84357949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36668077-T-G

84358122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36667896-A-G

84358451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36667637-C-G

84358451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36667637-C-T

84358464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36667624-G-A

http://identifiers.org/hco/10/GRCh38#84358480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36667608-A-C

84362204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36665821-G-A

84362269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36665751-C-T

84362486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36665530-A-G

84362606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36665422-T-G

84362713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36665330-A-G

84363370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36665185-G-A

84363380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36665174-G-A

84363435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36665111-G-A

84363435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36665111-G-T

84363632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36664927-T-A

84363632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36664927-T-G

84363687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36664874-G-A

84363688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36664873-C-G

84363688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36664873-C-T

84364422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36664747-G-C

84364442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36664727-G-T

http://identifiers.org/hco/10/GRCh38#84364664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36664525-A-C

84364664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36664525-A-G

84365301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36664214-A-T

84365402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36664121-G-T

84365412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36664113-A-T

84365425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36664100-C-T

84365467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36664045-A-G

84365719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36663809-T-C

84370761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36663452-T-G

84370899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36663299-A-G

84370899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36663299-A-T

84370927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36663286-T-A

84370927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36663286-T-C

84370930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36663283-A-G

84370930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36663283-A-T

84371016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, splice_region_variant
orthologous variants: 36663217-T-A

84371016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, splice_region_variant
orthologous variants: 36663217-T-G

84371093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: missense variant
orthologous variants: 36663140-A-G

http://identifiers.org/hco/10/GRCh38#84371231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/14/GRCm39#36663002-C-A

84371231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: missense variant
orthologous variants: 36663002-C-T

84371347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: missense variant
orthologous variants: 36662886-G-A

84371435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: missense variant
orthologous variants: 36662798-C-T

84371573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: missense variant
orthologous variants: 36662663-A-G

84371593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: missense variant
orthologous variants: 36662643-T-C

84371594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: missense variant
orthologous variants: 36662642-C-T

84371689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: missense variant
orthologous variants: 36662547-A-G

84371956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: missense variant
orthologous variants: 36662280-G-C

84371956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: missense variant
orthologous variants: 36662280-G-T

84371965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: missense variant
orthologous variants: 36662271-A-G

84371972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: missense variant
orthologous variants: 36662264-C-T

84372010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: missense variant
orthologous variants: 36662226-C-T

84372110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: missense variant
orthologous variants: 36662126-C-T

84372164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: missense variant
orthologous variants: 36662072-A-T

84372205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: missense variant
orthologous variants: 36662031-G-A

84372350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: missense variant
orthologous variants: 36661886-A-G

84372421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: missense variant
orthologous variants: 36661815-G-A

84372421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: missense variant
orthologous variants: 36661815-G-C

84372426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: synonymous variant
orthologous variants: 36661810-A-G

84372431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: missense variant
orthologous variants: 36661805-T-A

84372438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: synonymous variant
orthologous variants: 36661798-A-G

http://identifiers.org/hco/10/GRCh38#84372518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36661720-A-C

84372518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36661720-A-G

84372558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36661682-G-T

84372712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36661544-T-A

84372778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36661479-G-T

84372839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36661419-T-G

84372986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36661279-A-G

84373143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36661151-A-G

84373302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36661029-C-T

84373469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36660880-A-T

84373582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36660783-A-G

84373666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: missense variant
orthologous variants: 36660688-C-T

84373729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: missense variant
orthologous variants: 36660625-A-G

84373822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 36660532-A-G

84373830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 36660524-A-G

84373918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36660495-A-G

84373919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36660494-C-T

http://identifiers.org/hco/10/GRCh38#84374042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36660456-C-A

84374078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36660422-T-C

http://identifiers.org/hco/10/GRCh38#84374084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36660416-C-A

84374084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36660416-C-T

http://identifiers.org/hco/10/GRCh38#84374093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36660406-C-A

84374139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36660389-G-A

84374139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36660389-G-C

84374139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36660389-G-T

84374329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36660216-C-T

84374553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36659998-G-C

84374706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36659870-A-G

84374961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36659647-T-A

84375098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36659529-T-G

84375203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36659454-C-T

84375216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, undefined
orthologous variants: 36659442-C-G

84375337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36659314-G-A

84375595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36658997-T-C

84375710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36658888-T-A

84375715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36658883-T-A

84376025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36658611-A-G

84376236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36658329-G-A

84376346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36658241-A-G

84376425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36658120-C-T

http://identifiers.org/hco/10/GRCh38#84376597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36657876-C-A

84376600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36657873-G-A

84393797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36657586-A-G

84393800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron variant
orthologous variants: 36657583-T-C

http://identifiers.org/hco/10/GRCh38#84393975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36657410-C-A

84393975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36657410-C-T

http://identifiers.org/hco/10/GRCh38#84393995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36657387-C-A

http://identifiers.org/hco/10/GRCh38#84394041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36657302-A-C

84394049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36657292-G-T

84394481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36656793-A-G

84394607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36656677-G-A

84394657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36656629-A-G

http://identifiers.org/hco/10/GRCh38#84394786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36656491-A-C

84394788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36656489-C-T

84394832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36656442-T-C

84395550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36656054-A-G

84395690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36655922-C-T

http://identifiers.org/hco/10/GRCh38#84417758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36648897-C-A

84417758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36648897-C-T

84417789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36648866-G-A

84417789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36648866-G-C

84417789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 36648866-G-T

84417872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36648782-A-G

84417872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36648782-A-T

http://identifiers.org/hco/10/GRCh38#84417965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36648712-C-A

84418012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36648666-G-T

84419680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36647013-T-G

84419953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36646731-G-A

84419958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36646726-A-G

84420026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36646645-G-A

84420045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36646626-G-A

84420067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36646604-A-G

84420247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36646414-G-A

84420413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36646257-G-A

84420414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36646256-A-G

84420422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36646248-G-A

84420446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36646230-A-G

http://identifiers.org/hco/10/GRCh38#84420447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36646229-A-C

84420629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36646094-G-C

84421195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36645476-A-G

84424680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36641532-G-T

84424681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36641531-G-T

84424786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36641444-T-C

84424849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36641380-G-A

84424849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36641380-G-T

http://identifiers.org/hco/10/GRCh38#84424880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#36641349-C-A

84424880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36641349-C-G

http://identifiers.org/hco/10/GRCh38#84425013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36641215-A-C

84425013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36641215-A-G

84425022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36641206-T-C

84425036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36641192-A-G

84425057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36641171-A-G

84425102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36641129-T-C

84425254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36640982-G-T

http://identifiers.org/hco/10/GRCh38#84425342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36640888-C-A

84425855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36640427-T-C

84425862-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36640420-T-A

84425862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36640420-T-C

84425875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36640407-G-A

http://identifiers.org/hco/10/GRCh38#84425906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36640377-C-A

84425906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36640377-C-T

84425914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36640369-G-A

84425914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36640369-G-C

84425931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36640353-T-C

84425946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36640335-T-A

84425946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36640335-T-C

84425958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36640325-T-A

84425981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36640316-T-A

84425981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36640316-T-C

84426051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36640253-A-G

84426113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36640194-C-T

84426150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36640145-T-G

84426288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36640015-C-T

84426555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36639765-G-T

84426593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36639730-C-T

84426697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36639632-T-C

84428536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36636705-A-G

84428596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36636652-A-G

84429304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36636012-T-A

84429368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36635939-G-A

84429371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36635936-C-G

84437803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36631886-C-G

84437803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36631886-C-T

84437882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36631792-T-C

84437892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36631782-T-G

84438144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36631527-T-C

http://identifiers.org/hco/10/GRCh38#84438161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36631511-A-C

84438169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36631503-A-G

84438201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36631472-G-T

84438233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36631445-C-T

84438279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 36631395-C-T

http://identifiers.org/hco/10/GRCh38#84438362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36631306-C-A

84438398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36631275-T-G

84438468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36631203-G-A

84438468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36631203-G-C

84438468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36631203-G-T

84438666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36631013-G-C

84438713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36630966-T-A

http://identifiers.org/hco/10/GRCh38#84438715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36630964-C-A

84438715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 36630964-C-G

84438715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 36630964-C-T

84450683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36630064-T-G

84450795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36629955-A-G

84450989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36629822-A-G

84452119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36628556-A-G

http://identifiers.org/hco/10/GRCh38#84452181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36628289-A-C

84452181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36628289-A-G

http://identifiers.org/hco/10/GRCh38#84452194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36628276-C-A

84452194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36628276-C-T

84452225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36628245-C-G

84452228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36628242-G-A

84452228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36628242-G-T

84452243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36628227-G-A

84452295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36628175-G-A

84452295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36628175-G-T

84452445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36628032-G-T

84452875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36627202-T-C

84460975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36625796-T-C

84461084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36625698-C-G

84462343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36624636-G-A

84462374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36624606-G-A

84462384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36624596-T-C

84463298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36623375-C-T

84463691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36623007-A-G

84463694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36623004-C-T

84463699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36622999-T-C

http://identifiers.org/hco/10/GRCh38#84463815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36622892-C-A

84463869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36622863-G-A

84463869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36622863-G-C

84463869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36622863-G-T

http://identifiers.org/hco/10/GRCh38#84463876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36622856-C-A

84463876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36622856-C-T

84464054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36622679-T-C

84464055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36622678-T-C

http://identifiers.org/hco/10/GRCh38#84464121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36622370-A-C

84464121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36622370-A-G

84464139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36622352-T-G

84464703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36621848-C-T

84464906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36621680-G-C

http://identifiers.org/hco/10/GRCh38#84464909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36621677-C-A

84464909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36621677-C-G

84464909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36621677-C-T

http://identifiers.org/hco/10/GRCh38#84465112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36621495-C-A

84469769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36620796-C-T

84469939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36620587-T-C

84469968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36620558-T-A

84469972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36620554-G-T

84470043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36620500-G-T

84470341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36620230-T-C

84470384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 36620193-T-A

84470384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36620193-T-C

http://identifiers.org/hco/10/GRCh38#84470450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36620127-C-A

84470450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36620127-C-T

84471186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36619427-G-A

84476966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36619260-G-T

84477143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36618603-T-G

84477168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36618590-A-G

84477259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36618501-C-T

http://identifiers.org/hco/10/GRCh38#84477300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36618462-C-A

84477354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36618415-G-A

84477906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36617983-T-G

84478242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36617701-G-A

84478335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36617650-T-A

84478506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36617488-C-T

84478551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36617439-A-G

84478672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36617359-G-A

84478756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36617281-C-T

84479035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36617030-A-G

84482614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36614510-C-T

84482939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36614252-G-T

84483501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36614027-C-G

84499448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36612761-T-C

84499448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36612761-T-G

http://identifiers.org/hco/10/GRCh38#84499731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36612507-C-A

84499731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36612507-C-G

http://identifiers.org/hco/10/GRCh38#84499751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36612488-A-C

84499793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36612448-G-A

84499925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36612331-G-A

http://identifiers.org/hco/10/GRCh38#84499941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36612315-C-A

84499941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36612315-C-G

84500133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36612127-T-A

84500133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36612127-T-C

84500444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36611831-A-G

84500787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36611543-A-G

84500818-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36611512-T-A

84500818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36611512-T-C

84503268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36610544-C-T

84503577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36610227-G-A

84503837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36610010-G-T

84503876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36609944-A-T

84504880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36609604-G-A

http://identifiers.org/hco/10/GRCh38#84504957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36609533-A-C

http://identifiers.org/hco/10/GRCh38#84505033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36609474-C-A

84505475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36609119-G-A

http://identifiers.org/hco/10/GRCh38#84505611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36608980-A-C

84505880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36608722-C-T

http://identifiers.org/hco/10/GRCh38#84506012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36608632-A-C

84506071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36608602-T-G

http://identifiers.org/hco/10/GRCh38#84506131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36608550-C-A

84506899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36608124-C-T

84507241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36607798-G-A

84507241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36607798-G-C

84507241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36607798-G-T

http://identifiers.org/hco/10/GRCh38#84507358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36607680-C-A

84507358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36607680-C-G

84507373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36607665-A-G

84507373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36607665-A-T

84507381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36607657-T-G

84507721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36607336-T-C

84507738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36607319-G-A

84508023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36607085-G-T

84508273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36606837-A-G

84508277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36606833-A-G

84508448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36606705-T-C

84508729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36606433-T-C

84508836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36606321-C-T

84508941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36606231-T-G

84509457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36605749-A-G

84509503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36605703-C-T

84509975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36605213-T-A

84510004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36605159-G-A

84510063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36605107-T-A

84510070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36605100-C-T

84510086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36605090-A-G

84510148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36605029-T-C

84510449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36604761-A-G

84510800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36604657-C-T

84510803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36604654-C-G

84511165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36604343-C-T

84511241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36604269-A-T

84511364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36604172-G-C

84511495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36604081-T-C

84511631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36603958-C-T

84511721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36603892-C-T

84512435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36602733-G-T

84512498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36602709-G-A

84512572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36602646-C-T

84512604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36602617-G-A

84512604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36602617-G-C

84513100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36602042-C-G

84513418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36601746-T-C

http://identifiers.org/hco/10/GRCh38#84513421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36601743-C-A

84513469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, stop_gained, synonymous_variant
orthologous variants: 36601697-C-T

84513575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36601591-G-A

84513617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36601549-A-G

84513626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36601540-G-A

84513842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36601324-C-G

84513842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 36601324-C-T

84513998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36601189-G-A

84514067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36601120-C-T

84514160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36601027-C-T

84514283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36600907-C-G

84514283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36600907-C-T

84514306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36600884-A-G

84514488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36600715-T-A

http://identifiers.org/hco/10/GRCh38#84514533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36600674-C-A

84514533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36600674-C-G

84514533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36600674-C-T

84514637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36600582-G-A

84514637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36600582-G-T

84514708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36600511-G-A

84514715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36600504-G-A

84514715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36600504-G-C

http://identifiers.org/hco/10/GRCh38#84514885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36600334-C-A

84514923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36600297-T-C

84514923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36600297-T-G

84514949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36600270-A-G

http://identifiers.org/hco/10/GRCh38#84514950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36600269-C-A

84515144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36600122-T-A

84515239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36600021-G-A

84515807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36599765-G-T

84515831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36599736-T-C

84515896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36599673-T-G

84516103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36599475-T-A

84516103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36599475-T-C

84516170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36599417-G-A

84516337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36599260-C-T

84516351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36599246-G-A

84516351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36599246-G-T

84516360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36599238-A-G

84516498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36599101-A-G

http://identifiers.org/hco/10/GRCh38#84516506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36599094-C-A

http://identifiers.org/hco/10/GRCh38#84516549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36599042-A-C

84516599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36598995-A-T

84516706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36598894-C-T

84516950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36598407-G-A

84516971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36598392-A-T

84517013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36598350-A-T

84517132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36598235-G-C

84517155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36598212-A-G

84517256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36598126-T-C

84517299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36598065-T-C

84517589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36597765-G-A

84517589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36597765-G-T

84517792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36597567-G-T

http://identifiers.org/hco/10/GRCh38#84517820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36597539-C-A

84517837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36597524-G-A

84517980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36597422-T-C

84518003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: 36597399-T-G

http://identifiers.org/hco/10/GRCh38#84518070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29197
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#36597327-C-A