99659536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 5 prime UTR variant
orthologous variants: 43678285-A-G

99659536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 5 prime UTR variant
orthologous variants: 43678285-A-T

http://identifiers.org/hco/10/GRCh38#99659545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43678300-C-A

99659545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 5 prime UTR variant
orthologous variants: 43678300-C-T

99659609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43678364-G-A

99659609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43678364-G-C

99659609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43678364-G-T

99659614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43678369-G-A

99659614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43678369-G-C

99659614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43678369-G-T

99659696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43678452-C-T

99659726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 43678482-G-A

99659726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 43678482-G-C

99659726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 43678482-G-T

99659794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43678555-G-A

99659794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43678555-G-C

99659794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43678555-G-T

http://identifiers.org/hco/10/GRCh38#99659802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43678563-C-A

99660022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43678792-G-T

99660027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43678797-G-A

99660027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43678797-G-T

99660104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43678869-G-A

http://identifiers.org/hco/10/GRCh38#99660161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43678923-C-A

99660165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43678927-G-C

99661076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43679062-A-T

99661227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43679237-C-T

http://identifiers.org/hco/10/GRCh38#99661340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43679351-C-A

99661340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43679351-C-T

99661346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43679358-T-G

http://identifiers.org/hco/10/GRCh38#99661396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43679405-C-A

99661602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: synonymous_variant, undefined
orthologous variants: 43679613-A-G

99661679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43679779-T-C

99661712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43679886-G-T

99662164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43680621-C-T

99662455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43680903-T-C

99662461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43680909-C-T

99662492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43680940-T-A

99662511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43680961-A-G

99663122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43681133-A-G

99663129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43681140-C-G

99663248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43681268-T-C

99663423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43681397-A-T

http://identifiers.org/hco/10/GRCh38#99663722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43681496-A-C

99663921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43681638-A-G

99663961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43681680-T-C

99664006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43681719-G-T

99664143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43682022-C-G

99665334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43682463-G-A

99665401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43682534-C-G

99665421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43682554-G-C

99665463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43682592-G-A

99665463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43682592-G-T

99665549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43682646-T-C

99665852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43682732-C-T

99665937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43682813-T-C

99666108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43682979-G-A

99667085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43683886-G-A

99667313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43684139-T-C

99667332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43684170-T-C

99668615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43686063-A-T

99668836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43686452-T-G

99669017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43686637-G-T

99672734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43687228-A-G

99672754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43687245-T-C

99672808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43687295-T-C

99672952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43687441-A-G

99672962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43687451-C-T

99673016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43687503-A-T

99673040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43687527-A-G

99673465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43687956-A-G

99673527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43688029-A-G

http://identifiers.org/hco/10/GRCh38#99673624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43688170-A-C

99673624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43688170-A-G

99673706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43688252-A-G

99673813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43688355-C-G

99673834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43688376-T-G

99673949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43688476-G-A

99673981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43688494-G-T

99679580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43692954-A-G

99679580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43692954-A-T

99679681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43693084-G-A

http://identifiers.org/hco/10/GRCh38#99679693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43693290-A-C

99679801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: synonymous variant
orthologous variants: 43693395-T-C

99679807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: synonymous variant
orthologous variants: 43693401-T-C

99679840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: synonymous variant
orthologous variants: 43693434-C-T

99679849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: synonymous variant
orthologous variants: 43693443-A-G

http://identifiers.org/hco/10/GRCh38#99679895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43693491-A-C

99679895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43693491-A-G

99679895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43693491-A-T

http://identifiers.org/hco/10/GRCh38#99680003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43693606-C-A

http://identifiers.org/hco/10/GRCh38#99680004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43693607-C-A

99680004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43693607-C-T

http://identifiers.org/hco/10/GRCh38#99680016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43693619-C-A

99680016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43693619-C-T

99680350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43693929-G-A

99680466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43694048-T-A

99680491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43694073-C-T

99680579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43694155-C-T

99681736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: 43696287-G-T

99682233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43696665-A-T

99682334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43696791-A-G

99682411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43696874-A-G

99682680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43697100-C-T

99683017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43698005-G-A

99683022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: 43698010-G-T

99684867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43699477-T-C

99684871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43699481-C-T

99685326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43699635-G-A

99685538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43699819-A-G

99685737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43700039-T-C

http://identifiers.org/hco/10/GRCh38#99685834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43700216-A-C

99685834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: synonymous variant
orthologous variants: 43700216-A-T

http://identifiers.org/hco/10/GRCh38#99685940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43700359-C-A

99685940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43700359-C-T

99686012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43700549-T-C

99686023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43700560-G-T

99686207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43700761-T-C

99686517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43701525-C-T

99688636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43704655-G-T

99688710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: synonymous variant
orthologous variants: 43704729-T-A

99688795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43704806-G-A

99688818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43704827-A-G

99688828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43704837-T-C

99691345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43705841-T-G

99691375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43705879-T-C

99691533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43706037-A-G

99691559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43706060-A-G

99692175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43707425-T-C

99692213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43707465-C-T

http://identifiers.org/hco/10/GRCh38#99692221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43707473-C-A

99692366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43707499-G-A

99692576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43707689-G-T

99692642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43707755-G-A

99692654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43707767-G-A

99692855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43707928-T-A

99693202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43707971-C-G

99693202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43707971-C-T

99693322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43708098-T-C

99693382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43708150-A-G

99693466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43708227-C-T

http://identifiers.org/hco/10/GRCh38#99694874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43708812-A-C

99695074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43709002-A-G

99696021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 43710253-C-T

99696108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 43710340-T-C

99696219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43710421-G-T

99697050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43711095-T-C

99697105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43711150-G-A

99697172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43711216-C-T

99697287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43711313-A-G

99697440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: 43711552-T-C

http://identifiers.org/hco/10/GRCh38#99697484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#43711589-C-A

99697484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: 43711589-C-G

99697647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: 43711729-A-G

99697647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: 43711729-A-T

99697781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: 43711756-T-C

99697792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: 43711767-A-G

99697802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: 43711780-G-A

99697802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: 43711780-G-T

99697818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: 43711795-T-C

http://identifiers.org/hco/10/GRCh38#99698411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43713548-C-A

99698411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron variant
orthologous variants: 43713548-C-T

99698535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 43713654-T-C

99698535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 43713654-T-G

99698564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 43713683-C-T

99698610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, missense_variant
orthologous variants: 43713729-G-A

99698610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, missense_variant
orthologous variants: 43713729-G-T

99698626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, missense_variant
orthologous variants: 43713745-G-C

99698676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 43713795-A-G

99698717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 43713836-C-T

99698720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 43713839-A-G

99698741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 43713860-G-A

99698771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 43713890-C-T

99698780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 43713899-T-G

99699009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43714117-A-G

99699055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43714163-A-T

99699101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43714190-T-C

99699196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43714277-G-A

99699231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43714310-T-A

99699238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43714317-T-C

99699314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43714588-G-A

99699496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43714762-G-A

99699719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43714924-C-G

http://identifiers.org/hco/10/GRCh38#99700921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43715230-A-C

99700996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 43715305-G-A

99701090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43715399-G-A

99701090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43715399-G-C

99701090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43715399-G-T

http://identifiers.org/hco/10/GRCh38#99701092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43715401-C-A

99701159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43715469-G-A

99701161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43715471-G-A

99701161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43715471-G-T

http://identifiers.org/hco/10/GRCh38#99701188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43715499-C-A

99701275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43715574-T-G

99701518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43715765-G-C

99701777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43715934-G-A

99701777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43715934-G-T

99701785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43715942-C-T

99702090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43716094-T-C

99702242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43716189-T-G

99702530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 43716447-G-A

99702530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 43716447-G-T

http://identifiers.org/hco/10/GRCh38#99702728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#43716645-C-A

99702728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: 43716645-C-T

http://identifiers.org/hco/10/GRCh38#99702815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#43716696-A-C

99702815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: 43716696-A-T

99703043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: 43716935-G-A

99703210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: 43717103-T-C

99703267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: 43717146-C-T

99703318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: 43717197-A-G

99703482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: 43717359-A-G

99703482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: 43717359-A-T

99703724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: 43717607-A-T

99704210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: 43717908-G-A

99704242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: intron_variant, undefined
orthologous variants: 43717936-C-G

99704711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43718402-G-A

99704711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43718402-G-T

http://identifiers.org/hco/10/GRCh38#99704745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#43718448-C-A

99704808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43718492-T-C

99704817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43718497-T-C

http://identifiers.org/hco/10/GRCh38#99704822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#43718502-C-A

99704822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43718502-C-T

http://identifiers.org/hco/10/GRCh38#99704823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#43718503-C-A

99704823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43718503-C-T

99704962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43718632-G-A

http://identifiers.org/hco/10/GRCh38#99705038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#43718715-C-A

99705143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43718819-T-C

http://identifiers.org/hco/10/GRCh38#99705149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#43718825-A-C

99705149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43718825-A-G

http://identifiers.org/hco/10/GRCh38#99705545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#43719217-C-A

99705626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43719299-G-T

99705781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43719671-A-G

99705979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43719948-A-T

99706001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43719969-T-C

99709444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43721647-G-A

99709498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43721700-A-G

99709829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43722043-G-A

99709829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43722043-G-T

99709894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43722106-C-T

99709931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43722145-A-G

99710269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43722779-G-C

99710310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43722810-T-C

99710375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43722875-G-A

99710405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43722903-T-C

99710692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43723171-C-T

http://identifiers.org/hco/10/GRCh38#99710855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#43723539-C-A

99710929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19745
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43723614-G-C