116849572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 58931894-G-A

116849692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 58932014-C-T

http://identifiers.org/hco/10/GRCh38#116849716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58932038-C-A

116849725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 58932047-G-A

116849725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 58932047-G-C

116849725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 58932047-G-T

http://identifiers.org/hco/10/GRCh38#116849776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58932083-C-A

116849776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58932083-C-G

116849776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58932083-C-T

116849811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58932118-G-C

116849887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58932159-G-A

116849892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58932164-G-A

116849892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58932164-G-C

116849892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58932164-G-T

http://identifiers.org/hco/10/GRCh38#116849924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58932184-C-A

116849924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58932184-C-T

116850017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58932283-G-A

116850017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58932283-G-C

116850017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58932283-G-T

116850023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58932289-T-A

116850023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58932289-T-C

116850023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58932289-T-G

116850064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58932301-T-C

116850064-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58932301-T-G

http://identifiers.org/hco/10/GRCh38#116850091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58932328-C-A

116850091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 58932328-C-G

116850091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 58932328-C-T

http://identifiers.org/hco/10/GRCh38#116850107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58932341-C-A

116850133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58932367-C-T

116850141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58932375-A-G

116850190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58932413-G-T

116854269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58933479-G-T

116854500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58933710-C-T

116854552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58933758-T-C

116854587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58933792-A-G

116855499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58933883-G-A

116855545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58933923-G-A

116855545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58933923-G-C

http://identifiers.org/hco/10/GRCh38#116855658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58934001-C-A

116855658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58934001-C-T

116855673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58934016-G-A

116855786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58934133-T-C

116855850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58934200-G-A

116856312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58934898-A-G

http://identifiers.org/hco/10/GRCh38#116856356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58934944-C-A

116856356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58934944-C-T

116856515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58935107-G-A

116856515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58935107-G-T

116856576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, missense_variant
orthologous variants: 58935168-A-T

http://identifiers.org/hco/10/GRCh38#116856584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58935176-C-A

116856584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, missense_variant
orthologous variants: 58935176-C-G

116856584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58935176-C-T

116856599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58935191-C-T

116858695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58941287-A-G

http://identifiers.org/hco/10/GRCh38#116858978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58941557-C-A

http://identifiers.org/hco/10/GRCh38#116859066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58941642-C-A

116859066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, missense_variant
orthologous variants: 58941642-C-T

http://identifiers.org/hco/10/GRCh38#116859098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58941683-A-C

116859098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58941683-A-G

116859148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58941729-T-C

116859148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58941729-T-G

http://identifiers.org/hco/10/GRCh38#116859202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58941779-C-A

116859918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58942733-A-G

116859928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58942743-C-T

116859944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58942752-T-C

116860010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58942818-G-C

116860220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58943003-A-G

116860271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58943052-C-G

116860271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58943052-C-T

116860384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58943167-A-G

116860582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58943357-T-G

116860664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58943434-T-C

116860779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58943560-T-C

116860779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58943560-T-G

http://identifiers.org/hco/10/GRCh38#116860909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58943690-C-A

http://identifiers.org/hco/10/GRCh38#116860972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58943756-C-A

116860972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58943756-C-T

116860975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58943759-T-C

116861163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, missense_variant
orthologous variants: 58943954-A-G

http://identifiers.org/hco/10/GRCh38#116861260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58944041-C-A

116861260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58944041-C-T

116861278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58944060-T-G

116861289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58944068-T-A

116861375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58944151-A-G

116861553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58944304-C-T

116861706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58944436-C-G

116861789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58944526-C-G

116861805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58944534-A-G

116862098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58945350-C-G

http://identifiers.org/hco/10/GRCh38#116862686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58945903-C-A

116862686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58945903-C-T

116862767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58945990-A-G

116862852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 58946072-G-A

116862928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58946133-G-T

116862951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58946161-A-T

116868984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58947724-C-T

116869009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58947749-G-A

116870885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58948368-A-G

http://identifiers.org/hco/10/GRCh38#116870993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58948425-C-A

116870993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58948425-C-G

116870993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58948425-C-T

116871016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58948462-G-T

116871035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58948481-A-G

116871035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58948481-A-T

116871145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: missense variant
orthologous variants: 58948575-G-A

http://identifiers.org/hco/10/GRCh38#116871202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58948632-A-C

116871202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: synonymous variant
orthologous variants: 58948632-A-G

116871256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: synonymous variant
orthologous variants: 58948686-A-T

http://identifiers.org/hco/10/GRCh38#116871333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58948761-C-A

116871333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58948761-C-G

http://identifiers.org/hco/10/GRCh38#116871334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58948762-A-C

116871433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58948831-T-C

116871558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58949213-A-T

116871790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58949466-T-G

116871862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58949507-G-A

116873270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58950458-A-G

116873273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58950461-G-A

http://identifiers.org/hco/10/GRCh38#116873725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58950894-A-C

116873725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58950894-A-G

http://identifiers.org/hco/10/GRCh38#116873758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58950931-C-A

116873758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58950931-C-T

116873943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58951104-T-G

116873978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58951138-T-C

116874005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58951156-G-A

116874005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58951156-G-T

http://identifiers.org/hco/10/GRCh38#116874061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58951201-C-A

116874061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58951201-C-G

116874061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58951201-C-T

http://identifiers.org/hco/10/GRCh38#116874535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58951653-C-A

116874537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58951655-G-T

116875363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58952117-T-C

116875495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58952249-C-T

116875634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58952354-G-A

116875688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58952394-G-A

116875919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58952662-A-G

116875987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58952732-G-A

116875996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58952739-A-G

116876021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58952764-A-T

http://identifiers.org/hco/10/GRCh38#116876026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58952769-C-A

116876026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58952769-C-T

116876142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: synonymous variant
orthologous variants: 58952887-C-T

116876218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: missense variant
orthologous variants: 58952963-A-G

116876218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: missense variant
orthologous variants: 58952963-A-T

116876282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58953026-A-G

116876389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58953132-G-C

116876389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58953132-G-T

116876498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58953221-T-C

116877114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58953478-A-G

116878326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58956068-C-T

116878466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58956245-C-T

116878560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58956328-C-T

116878642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58956362-C-T

116878789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58956510-G-T

116878801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58956528-T-A

116878801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58956528-T-C

116878806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58956533-C-G

116878806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58956533-C-T

116878855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58956579-T-C

116878855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58956579-T-G

116878874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58956601-G-C

116878883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58956610-A-G

116878919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58956635-A-G

116878994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58956678-T-C

116879179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58956833-G-C

116879179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58956833-G-T

http://identifiers.org/hco/10/GRCh38#116879188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58956842-C-A

116879196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58956850-T-G

116879253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58956896-T-C

http://identifiers.org/hco/10/GRCh38#116879288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58956931-C-A

http://identifiers.org/hco/10/GRCh38#116879447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58957099-A-C

116879624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58957280-G-A

116879630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58957286-A-G

116879860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58957482-C-G

http://identifiers.org/hco/10/GRCh38#116880064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58957703-C-A

116880064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58957703-C-G

116880080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58957719-A-T

116880607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58958239-T-A

116880775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58958444-A-G

116880950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58958601-G-A

116880967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58958621-T-C

116881184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58958814-G-A

116881430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58958942-T-C

116881430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58958942-T-G

116881470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: 58958981-G-A

http://identifiers.org/hco/10/GRCh38#116881472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58958983-C-A

116881485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58958997-G-C

116881490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58959002-T-C

116881520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 58959053-A-G

116881602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 58959123-C-T

116881642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 58959163-A-G

http://identifiers.org/hco/10/GRCh38#116881694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58959210-C-A

116881694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58959210-C-T

http://identifiers.org/hco/10/GRCh38#116881733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58959245-C-A

116881733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58959245-C-T

116881810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58959332-T-C

http://identifiers.org/hco/10/GRCh38#116881897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58959404-C-A

116881897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58959404-C-T

http://identifiers.org/hco/10/GRCh38#116881940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58959450-A-C

116881940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58959450-A-G

116881958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58959470-T-A

http://identifiers.org/hco/10/GRCh38#116881962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58959474-C-A

116881962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58959474-C-T

http://identifiers.org/hco/10/GRCh38#116882169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58959704-C-A

http://identifiers.org/hco/10/GRCh38#116882338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58959860-C-A

http://identifiers.org/hco/10/GRCh38#116882367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58959889-C-A

116882432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58959925-A-G

116882618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960086-G-T

116882968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960399-A-G

http://identifiers.org/hco/10/GRCh38#116882995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58960411-C-A

116882995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960411-C-T

116883170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960536-T-C

116883191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960557-C-T

116883193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960559-A-G

116883263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960639-C-T

116883435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960694-T-A

http://identifiers.org/hco/10/GRCh38#116883553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58960728-C-A

116883651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960817-T-C

116883651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960817-T-G

http://identifiers.org/hco/10/GRCh38#116883673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58960833-C-A

116883673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960833-C-T

http://identifiers.org/hco/10/GRCh38#116883674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58960834-C-A

116883674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960834-C-T

116883682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960838-T-C

http://identifiers.org/hco/10/GRCh38#116883888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58960987-C-A

http://identifiers.org/hco/10/GRCh38#116883970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58961042-C-A

116884015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58961085-G-A

http://identifiers.org/hco/10/GRCh38#116884185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58961205-C-A

http://identifiers.org/hco/10/GRCh38#116884343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58961305-C-A

116884343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58961305-C-T

http://identifiers.org/hco/10/GRCh38#116884347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58961309-C-A

116884347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58961309-C-T

116884597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58961572-G-T

116884604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58961585-T-G

116884646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58961626-G-A

116884646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58961626-G-T

116884830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58961819-G-C

http://identifiers.org/hco/10/GRCh38#116884898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58961887-C-A

http://identifiers.org/hco/10/GRCh38#116884964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58961956-C-A

116884964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58961956-C-T

116885029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58962019-A-T

116885179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58962168-G-T

http://identifiers.org/hco/10/GRCh38#116885193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58962182-A-C

116885193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58962182-A-G

116885285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58962274-T-C

116885337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58962326-C-T

116885689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58962694-G-T

116885857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58962845-T-C

http://identifiers.org/hco/10/GRCh38#116885862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58962850-C-A

116885876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58962864-T-C

116885878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58962866-C-G

116885878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58962866-C-T

116885884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58962872-T-C

116885891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58962879-G-T

116885904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58962890-G-A

116885904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58962890-G-T

http://identifiers.org/hco/10/GRCh38#116886122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58963221-C-A

116886122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58963221-C-T

116886363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 58963437-G-A

116886363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 58963437-G-C

116886476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 58963550-A-G

116886585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58963658-G-A

116886585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58963658-G-C

116886622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58963696-T-C

116887022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58964101-G-A

116887071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58964160-G-C

116887090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58964181-G-A

116887305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58964392-G-C

116887354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58964498-A-G

116887650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58964781-T-C

http://identifiers.org/hco/10/GRCh38#116888536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58965396-C-A

http://identifiers.org/hco/10/GRCh38#116888583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58965439-C-A

116888585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58965442-A-T

116888713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58965585-C-G

116888717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58965589-T-A

116888734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58965606-C-G

116888752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58965620-G-A

116888854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58965714-T-G

116888863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58965723-C-T

116890125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58967089-A-G

116890262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58967219-C-T

116890296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58967273-T-C

116890359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58967338-T-C

116890390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58967366-G-C

http://identifiers.org/hco/10/GRCh38#116890792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58967706-C-A

116890838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58967749-G-C

116890858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58967771-A-G

http://identifiers.org/hco/10/GRCh38#116891724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58968657-A-C

116891911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58968799-G-T

116892095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58968927-G-A

116892095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58968927-G-C

116892281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58969071-C-G

116892409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58969158-T-C

116892638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58969399-T-C

116892642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58969403-T-C

116892703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58969473-G-A

116893170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58969959-G-T

http://identifiers.org/hco/10/GRCh38#116893541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58970337-C-A

116893541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58970337-C-T

116893575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58970406-T-C

116893763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58970613-A-G

116893774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58970628-T-C

116894040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58970848-T-C

116894256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58971069-C-T

116894298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58971116-G-A

116894298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58971116-G-T

116894422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58971256-T-C

http://identifiers.org/hco/10/GRCh38#116895370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58972379-A-C

116895852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58972835-C-G

116895852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58972835-C-T

116895952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58972948-C-T

116896193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58973175-A-G

116896201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58973183-C-T

116896702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58973587-C-T

116896768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58973650-G-C

116896791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58973668-T-C

http://identifiers.org/hco/10/GRCh38#116900194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58977137-C-A

116900194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58977137-C-T

116900304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58977247-T-C

116900578-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58977525-A-T

116900913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58977836-T-A

116900913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58977836-T-C

116901002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58977929-T-C

116901019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58977945-G-A

116901196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58978122-C-T

116901218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58978144-A-G

116901240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58978164-T-C

116901477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58978364-G-C

116901626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58978495-G-A

116901662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58978527-G-A

116901662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58978527-G-C

116901662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58978527-G-T

http://identifiers.org/hco/10/GRCh38#116901670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58978532-C-A

http://identifiers.org/hco/10/GRCh38#116901721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58978577-C-A

116901721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58978577-C-G

116901721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58978577-C-T

116901756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58978612-G-A

116901756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58978612-G-T

116902091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58978945-G-A

116902091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58978945-G-T

116902105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58978967-G-A

116902105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58978967-G-C

116902225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58979083-G-A

116902242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58979100-G-A

116902263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58979121-T-C

116902559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58979424-G-C

116902630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58979495-G-A

116902630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58979495-G-T

116903540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58980262-G-T

http://identifiers.org/hco/10/GRCh38#116903542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58980264-C-A

116903542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58980264-C-T

116903652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58980367-A-T

116903660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58980375-G-C

116903844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58980563-C-T

116903955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58980657-G-A

116904614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58981260-A-G

116904656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58981296-G-C

http://identifiers.org/hco/10/GRCh38#116904712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58981343-A-C

116904712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58981343-A-G

116904727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58981358-T-G

http://identifiers.org/hco/10/GRCh38#116904787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58981402-C-A

http://identifiers.org/hco/10/GRCh38#116906127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58982615-A-C

116906160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58982648-T-A

116906582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58983405-T-C

116906913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58983729-G-C

116907176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58983964-G-A

116907210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58983999-C-T

116907253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58984035-T-C

116907253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58984035-T-G

116907490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58984254-G-A

116907518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58984277-C-T

116907586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58984339-C-T

116907601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58984350-C-T

116907715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58984454-G-A

116907768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58984504-A-T

116907836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58984544-G-A

116907836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58984544-G-C

116907918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58984601-A-G

116907918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58984601-A-T

116908428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58985031-T-C

116908540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58985143-A-G

116908545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58985148-T-C

116908995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58985538-A-G

116909226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58985801-T-C

116909409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58985939-T-C

116909417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58985947-T-C

116910148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58986598-G-A

116910771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58987235-A-G

116911252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, undefined
orthologous variants: 58987688-G-A

116911567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 58988110-G-A

116911568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 58988111-T-C

116911590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58988133-A-T

116911624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58988153-T-C

116911666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58988205-C-G

116911666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58988205-C-T

http://identifiers.org/hco/10/GRCh38#116911888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58988425-A-C

116912246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31670
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58989296-C-T