http://identifiers.org/hco/15/GRCh38#39934152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118219150-C-A

39934152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: 5 prime UTR variant
orthologous variants: 118219150-C-T

39934163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: 5 prime UTR variant
orthologous variants: 118219161-G-A

39934163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: 5 prime UTR variant
orthologous variants: 118219161-G-T

39934240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: synonymous_variant, undefined
orthologous variants: 118219234-T-C

39934240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: synonymous_variant, undefined
orthologous variants: 118219234-T-G

http://identifiers.org/hco/15/GRCh38#39934387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118219373-C-A

39934387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118219373-C-G

39934387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118219373-C-T

http://identifiers.org/hco/15/GRCh38#39934456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118219433-C-A

39934480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118219455-T-G

39934637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118219581-C-G

39934637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118219581-C-T

39934643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118219587-C-T

39934855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118219757-G-A

39934855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118219757-G-C

39935785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118220118-C-T

39936007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118220320-A-G

39936009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118220322-G-C

http://identifiers.org/hco/15/GRCh38#39936015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118220328-A-C

39936015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118220328-A-G

39936135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118220443-G-A

39936152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118220460-C-T

39936205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118220539-C-T

39936359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118220690-A-G

http://identifiers.org/hco/15/GRCh38#39936398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118220736-A-C

39937158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118221185-T-C

39937183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118221207-T-A

39937285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118221300-G-C

39937684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118222131-G-A

39937684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118222131-G-T

39937815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118222230-T-C

39937907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118222368-A-G

39938020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118229957-C-T

39939151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118230406-C-T

39939391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118230633-A-G

39939468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118230748-G-A

http://identifiers.org/hco/15/GRCh38#39939496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118231007-C-A

39939496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118231007-C-T

39939587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: missense variant
orthologous variants: 118231098-G-A

http://identifiers.org/hco/15/GRCh38#39939600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118231111-A-C

39939681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, undefined
orthologous variants: 118231190-G-T

http://identifiers.org/hco/15/GRCh38#39939694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118231203-A-C

39939694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118231203-A-G

39939751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, undefined
orthologous variants: 118231270-A-G

39939762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, undefined
orthologous variants: 118231281-A-G

39939769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118231288-G-C

39939769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118231288-G-T

39940053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118231572-T-C

39940284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118231812-A-G

39940417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118231924-G-T

39940477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118231984-T-C

39941055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118232436-G-A

39941182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118232558-T-C

39941182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118232558-T-G

39941250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118232648-T-A

39941341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118232738-A-G

39941414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118232810-C-T

39941439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118232835-A-G

39941496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118232894-T-G

39941503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118232901-C-T

39941627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118233008-A-T

39942417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118234563-T-C

39942501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, undefined
orthologous variants: 118234655-C-T

39942661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118234819-G-A

http://identifiers.org/hco/15/GRCh38#39942841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118235027-C-A

http://identifiers.org/hco/15/GRCh38#39943056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118235144-C-A

39943121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118235204-T-C

39943198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118235287-C-T

39943232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118235329-C-T

39943253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118235351-A-T

39943398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: synonymous variant
orthologous variants: 118235543-G-A

39943398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: missense variant
orthologous variants: 118235543-G-T

39947120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118236690-G-A

39947267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118236829-T-G

39947645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118237502-C-G

39947736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118237561-G-A

39947916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118237725-C-T

39948124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118237910-T-C

39948258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118238020-C-T

http://identifiers.org/hco/15/GRCh38#39948321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118238073-A-C

39948326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118238078-A-G

39948417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118238162-C-G

http://identifiers.org/hco/15/GRCh38#39948609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118238325-A-C

39948747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118238454-G-A

39948987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118238697-T-C

39948988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118238698-A-G

39949023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118238735-G-A

39949023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118238735-G-T

39949151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: synonymous variant
orthologous variants: 118238868-A-G

39949251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: missense variant
orthologous variants: 118238968-C-T

39949318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118239028-C-T

39949443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118239161-A-G

39949449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118239167-G-A

39951883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118239885-C-T

39952263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118240364-G-A

39952263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118240364-G-T

39952682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118240584-T-C

39953208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118240797-G-C

39953239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118240827-A-G

39953426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118240999-A-G

39953464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118241038-C-T

39953512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118241081-C-T

39953521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118241087-C-T

39953632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118241181-T-G

39953758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118241236-T-C

39953758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118241236-T-G

39953862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118241320-G-A

39954013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118241472-T-C

39954014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118241473-A-G

39954047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118241505-T-A

39954047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118241505-T-C

39954090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118241717-G-A

39954090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118241717-G-T

39954129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118241766-T-C

39954129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118241766-T-G

39954155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118241792-G-A

39954224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118241864-G-C

39954636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118241968-C-T

39954756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118242020-G-A

http://identifiers.org/hco/15/GRCh38#39955094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118242259-C-A

39955094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118242259-C-T

39955215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118242363-A-G

39955559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118243356-A-G

39955603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118243399-T-C

39955603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118243399-T-G

39955706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: synonymous variant
orthologous variants: 118243502-T-C

http://identifiers.org/hco/15/GRCh38#39955749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118243545-A-C

39955892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118243674-A-G

http://identifiers.org/hco/15/GRCh38#39955902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118243684-A-C

39956044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118243791-C-T

http://identifiers.org/hco/15/GRCh38#39956045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118243792-A-C

http://identifiers.org/hco/15/GRCh38#39956056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118243803-A-C

39959855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118246153-T-C

39959867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118246165-G-A

http://identifiers.org/hco/15/GRCh38#39960378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118246344-A-C

39960517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118246449-G-T

39960663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118246563-A-T

39960737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118246629-A-G

39960768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118246659-G-A

39960768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118246659-G-T

39960851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118246734-A-G

39960874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118246757-G-C

39960974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118246845-A-T

39960976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118246847-C-T

39961168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118247068-G-A

39961673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118247646-G-A

39961673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118247646-G-T

39961810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: missense variant
orthologous variants: 118247734-A-G

39961810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: missense variant
orthologous variants: 118247734-A-T

http://identifiers.org/hco/15/GRCh38#39961919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118247843-C-A

39962005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118247926-G-A

39962021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118247942-G-A

39962021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118247942-G-T

39962309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118248038-A-G

39962653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118248260-A-G

39962989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118248549-G-A

39963169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118248723-C-T

39963223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118248746-G-A

39963225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118248748-G-C

39963538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118249001-A-G

39963655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118249123-G-C

39963783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118249234-T-C

39963892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118249482-T-C

39964084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118249717-G-A

39964257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118249892-T-C

39964464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118250493-G-A

39964470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118250499-G-A

39964658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118250644-T-C

39964750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118250716-C-T

39964775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118250736-G-A

39965546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118251113-T-C

39965547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118251114-A-G

http://identifiers.org/hco/15/GRCh38#39965560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118251127-C-A

39965657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118251171-T-G

39965853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118251367-C-G

39965869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118251383-G-T

39967168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118252340-G-A

http://identifiers.org/hco/15/GRCh38#39967297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118252416-A-C

39967297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118252416-A-G

39967496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: missense variant
orthologous variants: 118252596-C-G

39967496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: synonymous variant
orthologous variants: 118252596-C-T

39967778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: synonymous variant
orthologous variants: 118252878-T-C

39967778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: synonymous variant
orthologous variants: 118252878-T-G

39967904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118253000-A-G

39967905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118253001-A-G

39967969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118253038-G-A

39967969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118253038-G-C

39967969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118253038-G-T

http://identifiers.org/hco/15/GRCh38#39967990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118253065-C-A

39968030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118253088-G-A

39968030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118253088-G-T

39968365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118253415-A-G

39968433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118253724-T-C

39968448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118253738-A-G

39968466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118253756-C-T

39969082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118254919-A-T

39969136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118254971-G-C

39970318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118255428-T-C

39970362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118255471-T-A

39972581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118256721-G-A

39972589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118256729-A-G

39972619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118256759-A-G

39972828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118256971-A-G

http://identifiers.org/hco/15/GRCh38#39972830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118256973-C-A

39972830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118256973-C-T

39972980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: missense variant
orthologous variants: 118257118-G-C

39972986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: synonymous variant
orthologous variants: 118257124-A-G

39973027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118257597-C-T

39973082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118257642-A-G

39973131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118257696-A-G

39973153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118257715-T-A

39973153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118257715-T-G

39973203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118257767-T-C

39973235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118257795-T-C

39973255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118257810-T-C

39973445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118257970-A-G

39973620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: synonymous variant
orthologous variants: 118258337-T-C

39973771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, missense_variant
orthologous variants: 118258486-A-G

http://identifiers.org/hco/15/GRCh38#39973777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118258492-C-A

39973777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, missense_variant
orthologous variants: 118258492-C-T

39973893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118258605-T-C

39974037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118258761-A-G

39974095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118258810-T-C

39974482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118259180-C-G

39975722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118260202-A-G

39975809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118260295-T-C

39976107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118260618-T-G

39976340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118261192-G-A

39976340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118261192-G-T

39976389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118261241-T-C

39976406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 118261269-T-G

39976459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: missense variant
orthologous variants: 118261322-C-G

39976459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: missense variant
orthologous variants: 118261322-C-T

39976478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: missense variant
orthologous variants: 118261341-G-A

39976478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: missense variant
orthologous variants: 118261341-G-C

39976491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: missense variant
orthologous variants: 118261354-G-C

39976521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: synonymous_variant, undefined
orthologous variants: 118261384-G-A

39976521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: synonymous_variant, undefined
orthologous variants: 118261384-G-C

39976599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: synonymous_variant, undefined
orthologous variants: 118261462-G-A

39976599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: synonymous_variant, undefined
orthologous variants: 118261462-G-T

39976643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: missense_variant, undefined
orthologous variants: 118261506-G-A

39976643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: missense_variant, undefined
orthologous variants: 118261506-G-T

http://identifiers.org/hco/15/GRCh38#39976794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118261657-C-A

39976794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: synonymous variant
orthologous variants: 118261657-C-T

http://identifiers.org/hco/15/GRCh38#39977110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118261768-A-C

39977110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118261768-A-G

39977110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118261768-A-T

39977122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118261780-T-A

39977122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118261780-T-C

39977122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118261780-T-G

http://identifiers.org/hco/15/GRCh38#39977126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118261784-C-A

39977126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118261784-C-T

http://identifiers.org/hco/15/GRCh38#39977149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118261799-A-C

39977149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118261799-A-G

http://identifiers.org/hco/15/GRCh38#39977577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118261873-C-A

http://identifiers.org/hco/15/GRCh38#39977827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118262079-C-A

39977827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118262079-C-G

39977827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118262079-C-T

http://identifiers.org/hco/15/GRCh38#39977847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118262099-C-A

39977847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118262099-C-T

39977861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118262113-G-A

39977861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118262113-G-C

39977861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118262113-G-T

39977994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118262612-T-C

39977994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118262612-T-G

39978036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118262651-A-G

39978037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118262652-G-T

39978055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118262666-G-A

39978055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118262666-G-T

39978057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118262668-A-G

39978170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118262784-T-C

39978170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118262784-T-G

39978183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118262800-G-A

39978183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118262800-G-C

39978183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118262800-G-T

http://identifiers.org/hco/15/GRCh38#39978199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118262825-C-A

39978227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118262852-T-A

39978227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118262852-T-C

39981431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118263907-G-A

39981591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118264071-T-C

39981613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118264093-T-C

39981757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118264610-T-C

39981762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118264615-T-A

http://identifiers.org/hco/15/GRCh38#39981813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118264656-A-C

39985665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118264959-G-A

39985665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118264959-G-T

39985766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118265068-G-A

39985825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, missense_variant
orthologous variants: 118265124-G-T

39985841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, missense_variant
orthologous variants: 118265140-A-G

http://identifiers.org/hco/15/GRCh38#39985924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118265223-C-A

39985924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118265223-C-T

http://identifiers.org/hco/15/GRCh38#39986038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118265503-C-A

39986038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118265503-C-T

http://identifiers.org/hco/15/GRCh38#39986039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118265504-C-A

39987813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118266317-G-A

http://identifiers.org/hco/15/GRCh38#39987955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118266614-C-A

39988006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: synonymous variant
orthologous variants: 118266667-T-A

39988051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: synonymous variant
orthologous variants: 118266712-A-G

39988120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118266781-A-G

39988120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118266781-A-T

39989028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118268415-G-A

39989058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118268441-A-T

39989566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118268795-C-T

39989857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269103-A-G

39989949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269191-G-T

39990012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269236-C-T

39990159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269329-T-C

39990169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269339-G-T

39990194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269363-G-A

39990194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269363-G-C

39990198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269367-G-A

39990198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269367-G-T

39990209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269379-T-G

39990210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269380-A-G

39990233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269406-A-G

39990249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269422-T-A

39990384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 118269588-A-G

http://identifiers.org/hco/15/GRCh38#39990471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118269670-A-C

http://identifiers.org/hco/15/GRCh38#39990473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118269672-C-A

39990473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269672-C-T

39990477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269676-G-A

39990477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269676-G-T

http://identifiers.org/hco/15/GRCh38#39990491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118269690-A-C

39990491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269690-A-G

39990491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269690-A-T

http://identifiers.org/hco/15/GRCh38#39990507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118269705-C-A

39990507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269705-C-G

39990515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269713-G-A

39990515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269713-G-T

39990519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269717-G-A

39990519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269717-G-T

39990702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118269865-A-G

39990913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118270261-G-A

39991023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118270358-G-C

39991094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118270406-T-G

39991100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118270412-A-T

39991116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118270428-G-A

39991116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118270428-G-T

http://identifiers.org/hco/15/GRCh38#39991123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118270435-C-A

39991123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118270435-C-T

39991147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron variant
orthologous variants: 118270459-A-G

39991304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118270775-G-A

39991304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118270775-G-T

http://identifiers.org/hco/15/GRCh38#39991334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118270802-C-A

39991334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118270802-C-G

39991348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118270816-T-G

39991407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118270852-A-G

39991422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118270867-A-T

39991487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118270914-C-T

39991571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118270983-G-A

39991910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118271340-T-C

http://identifiers.org/hco/15/GRCh38#39991997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118271423-C-A

39991997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118271423-C-T

39992024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118271450-T-C

39992069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118271505-T-C

39992148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118271608-G-T

39992157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118271617-G-C

39992314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118271780-G-T

http://identifiers.org/hco/15/GRCh38#39992328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118271794-C-A

39992328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118271794-C-T

http://identifiers.org/hco/15/GRCh38#39992547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118271989-C-A

http://identifiers.org/hco/15/GRCh38#39992583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118272009-A-C

39992583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118272009-A-G

39992583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118272009-A-T

http://identifiers.org/hco/15/GRCh38#39992588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118272014-A-C

39992588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118272014-A-G

39992653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118272086-G-A

39992653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118272086-G-T

39992656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118272089-A-G

39992800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118272527-C-T

39992867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118272622-A-G

39992894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118272652-G-A

39992930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118272689-G-A

39992930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118272689-G-T

39992992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118272742-G-T

39996832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118273521-G-A

39996832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118273521-G-C

39996832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118273521-G-T

39996981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118273623-C-T

http://identifiers.org/hco/15/GRCh38#39997092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118273735-C-A

39997092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118273735-C-G

39997106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118273749-G-A

39997106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118273749-G-T

http://identifiers.org/hco/15/GRCh38#39997108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118273751-A-C

39997112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118273755-T-C

39997114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118273756-A-G

39997159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118273797-T-C

http://identifiers.org/hco/15/GRCh38#39997214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118273975-C-A

39997214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118273975-C-T

39997409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118274145-G-A

39997426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118274162-A-G

39997744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118274418-T-C

39997935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118274596-A-G

39998006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118275966-T-A

39998174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118276120-G-A

39998703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118276710-C-T

http://identifiers.org/hco/15/GRCh38#39998808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118276818-C-A

39998808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118276818-C-G

http://identifiers.org/hco/15/GRCh38#39998825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118276834-C-A

39998877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118276886-T-A

39998877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118276886-T-C

39998877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118276886-T-G

39998891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118276900-G-T

39998892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118276901-G-A

39998892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118276901-G-T

39998900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118276909-G-A

39998900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118276909-G-T

39999221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277300-C-G

39999238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277316-A-G

39999256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277334-C-T

39999296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277377-G-A

39999361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277435-T-C

39999454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277541-A-G

http://identifiers.org/hco/15/GRCh38#39999602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118277668-A-C

39999602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277668-A-G

39999649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277717-T-G

39999680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277748-A-G

39999701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277769-T-G

39999710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277778-A-G

39999813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277910-A-G

39999833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277918-G-A

40000051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278022-A-G

40000235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278161-T-G

40000236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278162-T-A

40000241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278167-G-A

40000245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278171-T-A

40000278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278200-T-C

40000448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278310-T-C

40000511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278355-A-G

40000633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278456-G-A

40000633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278456-G-T

http://identifiers.org/hco/15/GRCh38#40000656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118278475-C-A

40000860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278661-A-G

40000860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278661-A-T

40000869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278671-G-T

40000878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278680-A-T

40000901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278687-G-T

http://identifiers.org/hco/15/GRCh38#40000909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118278694-C-A

40000909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278694-C-G

http://identifiers.org/hco/15/GRCh38#40000913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118278698-C-A

40000946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278716-T-C

40000970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278741-G-A

40001074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118278843-A-G

40001231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118278998-T-C

40001335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118279439-A-G

http://identifiers.org/hco/15/GRCh38#40001355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118279459-C-A

40001372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118279481-T-A

40001785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118279797-G-A

40001785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118279797-G-C

http://identifiers.org/hco/15/GRCh38#40001855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118279864-A-C

40002826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280895-T-A

40002831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280900-C-T

40002905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281625-T-C

http://identifiers.org/hco/15/GRCh38#40002949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118281657-A-C

40003047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281751-A-G

40003047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281751-A-T

40003254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118281954-C-T

40003379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118282035-G-A

40003379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118282035-G-C

40003379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118282035-G-T

http://identifiers.org/hco/15/GRCh38#40003465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118282124-A-C

40003465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118282124-A-T

40003757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118282312-C-T

40003839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118282384-A-G

40003963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118282590-T-C

40004022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118282647-A-G

40004090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118282801-A-T

40004147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118282896-G-A

40004238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118283021-T-A

40004251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118283034-T-C

40004360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118283132-A-T

40004400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118283170-T-C

40004498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118283271-C-T

40005324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118283636-G-T

40006972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285268-G-T

40006985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285281-A-G

40006986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285282-T-C

http://identifiers.org/hco/15/GRCh38#40007128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118285415-C-A

40007128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285415-C-G

40007352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285655-G-A

40007369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285674-A-G

http://identifiers.org/hco/15/GRCh38#40007380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118285685-C-A

40007380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285685-C-G

40007733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285983-G-C

http://identifiers.org/hco/15/GRCh38#40007880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118286121-C-A

40007880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286121-C-G

40007880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286121-C-T

http://identifiers.org/hco/15/GRCh38#40007906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118286147-C-A

40007906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286147-C-T

40007908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286148-T-C

40007909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286149-G-A

40007909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286149-G-T

http://identifiers.org/hco/15/GRCh38#40007987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118286218-A-C

40007987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286218-A-G

40007987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286218-A-T

40007996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286227-T-C

http://identifiers.org/hco/15/GRCh38#40007999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118286230-C-A

40007999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286230-C-G

40007999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286230-C-T

http://identifiers.org/hco/15/GRCh38#40008205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118286435-C-A

40008205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286435-C-T

http://identifiers.org/hco/15/GRCh38#40008215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118286445-C-A

http://identifiers.org/hco/15/GRCh38#40008245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118286462-C-A

40008251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286468-G-A

40008251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286468-G-C

40008251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286468-G-T

40008514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286732-C-T

40008519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286737-G-A

40008639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286831-G-T

40008774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286958-G-C

40008894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118287062-G-A

40008924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118287081-A-G

40008958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118287114-A-G

40009025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118287183-A-G

40009025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118287183-A-T

40009520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118287514-G-A

40009568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118287560-G-C

40009568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118287560-G-T

40009593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118287584-T-C

http://identifiers.org/hco/15/GRCh38#40009685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118287678-A-C

40009772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118287748-G-C

40009772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118287748-G-T

40009806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118287782-T-C

40010850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118288130-C-T

40011364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118288390-G-A

40011395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118288421-A-G

http://identifiers.org/hco/15/GRCh38#40011412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118288438-C-A

40011431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118288457-G-A

40011431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118288457-G-C

40011765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118288771-T-C

40012179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118290258-C-G

40012853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118290808-C-G

40012875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118290831-T-C

40013007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118290941-T-C

40016070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118291761-G-A

40016109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118291807-T-C

40016291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118291955-A-T

http://identifiers.org/hco/15/GRCh38#40016397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118292059-C-A

40016397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118292059-C-G

40016397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118292059-C-T

http://identifiers.org/hco/15/GRCh38#40016419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118292095-C-A

40016422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118292098-C-T

40016424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118292100-G-C

40016430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118292113-G-A

40016439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118292135-C-T

40016508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 118292214-C-T

40016525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 118292231-T-C

40016550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118292256-C-G

40016710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118292416-A-G

40016711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118292417-G-A

40016759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118292458-A-G

40016766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118292465-G-T

http://identifiers.org/hco/15/GRCh38#40016971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118292596-C-A

40017094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118292691-A-G

40017095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118292692-T-C

40017218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118292815-A-G

40017221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118292818-T-G

http://identifiers.org/hco/15/GRCh38#40017256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118292855-C-A

40017353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118292950-G-C

40017361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118292958-T-C

40019070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118293125-T-C

40019143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118293195-T-C

40019178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118293230-C-G

40019178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118293230-C-T

40020713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294259-G-C

40020713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294259-G-T

http://identifiers.org/hco/15/GRCh38#40020738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118294285-A-C

40020738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294285-A-G

40020738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294285-A-T

40020743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294290-G-A

40020743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294290-G-T

http://identifiers.org/hco/15/GRCh38#40020766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118294314-C-A

40020766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294314-C-T

40020797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294343-T-C

40020797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294343-T-G

40020802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294348-A-G

40020830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294358-T-C

40020870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294399-T-C

40020871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294400-A-G

http://identifiers.org/hco/15/GRCh38#40020873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118294405-C-A

40020873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294405-C-T

40021053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118294577-G-A

40021149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118295571-G-A

40021149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118295571-G-T

40021159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118295581-G-A

40021159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118295581-G-T

40021293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118295696-C-G

40021415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118295792-T-A

40021422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118295801-G-A

40021422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118295801-G-C

40021422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118295801-G-T

40021653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296000-A-G

40021672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296018-G-T

40021677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296023-G-A

40021677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296023-G-T

40021743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296092-G-A

40021743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296092-G-T

40021758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296103-C-T

40021965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296251-G-A

40021965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296251-G-C

40021965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296251-G-T

http://identifiers.org/hco/15/GRCh38#40022006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118296283-A-C

http://identifiers.org/hco/15/GRCh38#40022096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118296374-C-A

40022096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296374-C-T

http://identifiers.org/hco/15/GRCh38#40022140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118296442-A-C

40022140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296442-A-G

40022140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296442-A-T

40022142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296444-T-C

http://identifiers.org/hco/15/GRCh38#40022172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118296474-C-A

40022172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296474-C-G

40022172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296474-C-T

40022174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296476-T-C

http://identifiers.org/hco/15/GRCh38#40022261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118296580-C-A

40022261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296580-C-T

40022306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296633-A-G

40022306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296633-A-T

40022311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296638-T-A

40022311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296638-T-C

40022311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296638-T-G

40022320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296647-G-A

http://identifiers.org/hco/15/GRCh38#40022360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118296683-A-C

40022360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296683-A-G

40022360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296683-A-T

40022483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296804-T-A

40022495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118296816-C-T

http://identifiers.org/hco/15/GRCh38#40025832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118298498-C-A

40029091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118300417-G-A

40029140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118300465-C-T

40029536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118300851-A-G

40029614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118300920-G-A

40029614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118300920-G-T

http://identifiers.org/hco/15/GRCh38#40030257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118301224-C-A

http://identifiers.org/hco/15/GRCh38#40032035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118302264-C-A

40032035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118302264-C-G

40032035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118302264-C-T

40032337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118302536-T-C

40032339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118302538-G-T

40032546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118302714-G-C

http://identifiers.org/hco/15/GRCh38#40032650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118302931-C-A

40032650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118302931-C-G

40032650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118302931-C-T

http://identifiers.org/hco/15/GRCh38#40032703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118303032-C-A

40032703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118303032-C-T

40032716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118303049-T-C

40033053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118303291-C-T

40033238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118303364-G-C

http://identifiers.org/hco/15/GRCh38#40034261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118304450-C-A

40034261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118304450-C-T

http://identifiers.org/hco/15/GRCh38#40034309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118304497-A-C

40034309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118304497-A-G

40034400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118304587-C-T

http://identifiers.org/hco/15/GRCh38#40034911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118305393-C-A

40034911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118305393-C-G

40035021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118305478-T-C

40035097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118305554-G-A

40035097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118305554-G-T

40035125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118305581-G-A

40035125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118305581-G-C

40035125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118305581-G-T

40035588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19687
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118305712-T-G