190317938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26186383-T-A

190318232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26186663-G-A

190318294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26186734-T-G

190319489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26187946-A-T

190319506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26187958-T-C

190319647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26188101-G-A

190321574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26189756-A-T

190321974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26190144-G-A

http://identifiers.org/hco/3/GRCh38#190322278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#26190443-C-A

190322278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26190443-C-G

190322278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26190443-C-T

190322336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26190501-G-A

190322336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26190501-G-C

190322336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26190501-G-T

190322395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26190553-T-A

190322395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26190553-T-C

190322395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26190553-T-G

190322447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, undefined
orthologous variants: 26190592-G-A

190322447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, undefined
orthologous variants: 26190592-G-T

190322563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26190702-G-C

http://identifiers.org/hco/3/GRCh38#190322574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#26190718-C-A

190322574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26190718-C-T

190322611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26190756-G-T

190322630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26190764-G-A

190322630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26190764-G-T

190322644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26190778-G-A

190322644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26190778-G-T

http://identifiers.org/hco/3/GRCh38#190322708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26190842-A-C

190322708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26190842-A-G

http://identifiers.org/hco/3/GRCh38#190322719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26190854-C-A

190322719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26190854-C-T

http://identifiers.org/hco/3/GRCh38#190322796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26190932-C-A

190322796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26190932-C-T

http://identifiers.org/hco/3/GRCh38#190322831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26190964-C-A

190322831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26190964-C-T

190322986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26191132-C-G

190323040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26191143-G-A

190323040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26191143-G-T

190323087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26191187-C-T

190323143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26191216-G-T

190323172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26191254-A-G

190323199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26191350-C-G

190323228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26191377-C-T

190323357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26191471-A-G

190323509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26191613-T-C

190323905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26191988-T-A

190323905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26191988-T-C

190324022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26192152-G-A

190324076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26192178-G-A

190324076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26192178-G-T

190324698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26192411-A-G

190324760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26192468-G-C

190324829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26192535-C-T

190324996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26192705-A-G

190325155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26192840-T-C

190325327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26193020-T-A

190325485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26193161-T-C

190325821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26193842-C-T

190325822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26193843-G-A

190325962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26193963-G-T

http://identifiers.org/hco/3/GRCh38#190325996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26193994-C-A

190326096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26194575-T-A

190326221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26194674-A-G

190326374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26195302-G-T

190326473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26195398-C-G

190326482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26195407-G-T

190326485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26195410-T-G

190326665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26195545-T-C

http://identifiers.org/hco/3/GRCh38#190326813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26195696-A-C

190326813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26195696-A-G

190326900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26195806-A-G

190326901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26195808-G-A

190326908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26195815-T-C

190326969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26195877-T-A

190327001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26195910-G-A

190327402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26196272-A-G

190327504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26196359-G-C

190327570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26196421-C-T

190327592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26196443-G-A

190327730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26196539-G-A

190327779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26196582-G-A

190327817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26196620-G-A

190327901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26196704-C-T

190327920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26196723-G-T

190329134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26197844-G-T

190329410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26198105-G-A

http://identifiers.org/hco/3/GRCh38#190329450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26198142-C-A

190329450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26198142-C-T

190329522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26198212-C-T

190329572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26198288-A-G

190329572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26198288-A-T

190329643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26198355-G-A

190329672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26198387-C-T

190330552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26202397-T-C

190330573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26202422-G-T

190330674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26202510-C-T

http://identifiers.org/hco/3/GRCh38#190330736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26202571-C-A

190330752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26202587-G-A

http://identifiers.org/hco/3/GRCh38#190330835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26202669-C-A

190330835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26202669-C-G

190331015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26202948-A-G

190331162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26203101-G-A

190331190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26203129-A-G

190331197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26203136-T-C

http://identifiers.org/hco/3/GRCh38#190331292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#26203222-A-C

190331351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26203281-C-T

190331885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26203750-G-T

190331926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26203772-G-A

http://identifiers.org/hco/3/GRCh38#190331930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26203775-A-C

190331931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26203776-T-G

190332000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26203895-T-A

190332000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26203895-T-G

190332036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26203927-G-A

190332036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26203927-G-C

190332052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26203945-C-T

190332114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26204008-C-T

http://identifiers.org/hco/3/GRCh38#190332203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26204096-A-C

190332269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26204161-G-C

190332363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26204398-A-G

190332518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26204743-C-G

190332532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26204757-G-A

190332737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26204951-T-C

190332793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26204967-A-G

190332793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26204967-A-T

http://identifiers.org/hco/3/GRCh38#190332801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26204975-C-A

190332801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26204975-C-T

190332925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26205158-T-C

190333121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26205510-A-G

190333511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26205999-T-C

190333664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26206372-C-T

http://identifiers.org/hco/3/GRCh38#190335806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26208841-C-A

190335806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26208841-C-G

190335807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26208842-A-G

190335843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26208857-T-G

190335913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26208925-A-G

190336404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26209414-C-T

190336613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26209624-G-A

190336615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26209626-T-G

http://identifiers.org/hco/3/GRCh38#190336861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26209891-C-A

190336963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26209983-C-T

http://identifiers.org/hco/3/GRCh38#190337001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26210023-A-C

190337081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26210093-C-T

190337115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26210131-G-A

190339551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26214864-G-A

http://identifiers.org/hco/3/GRCh38#190339626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26214935-C-A

190339647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26214956-G-A

190339647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26214956-G-T

190339671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26214979-A-G

190339805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26215092-T-C

190339832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26215117-A-G

190344656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26219316-T-G

190344697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26219357-G-A

190344715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26219375-A-G

190344762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26219422-A-G

190344953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26219611-A-T

190345444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26220032-G-T

190345741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26220310-A-T

190345753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26220322-C-T

190352010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26225344-G-A

190352376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26225925-T-C

190352645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26226145-T-C

http://identifiers.org/hco/3/GRCh38#190352647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26226147-C-A

190355448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26233561-C-T

190355525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26233882-T-C

190355744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26235273-G-A

http://identifiers.org/hco/3/GRCh38#190355771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26235299-C-A

190355771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26235299-C-G

http://identifiers.org/hco/3/GRCh38#190355864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26235382-C-A

190355864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26235382-C-T

190355867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26235385-A-T

190355984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26235479-G-A

190356090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26235513-T-A

190356098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26235521-A-T

http://identifiers.org/hco/3/GRCh38#190356259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26235678-A-C

190356387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26235806-A-G

190356626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26236039-G-A

190356954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26237122-G-T

190357106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26237384-C-G

190357183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26237461-G-A

190357337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26237619-T-C

190357520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26237775-T-C

190366983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26242438-G-C

190367125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26242581-A-G

http://identifiers.org/hco/3/GRCh38#190367337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26242799-C-A

190367484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26242942-A-G

190367487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26242945-C-T

190367488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26242946-C-T

190367507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26242965-G-A

190367551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26242996-T-A

190367554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26242999-T-G

190367668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26243094-T-C

190367734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26243148-G-T

190369585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26248811-T-C

190369613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26248839-T-G

190369760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26249011-G-A

190369966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26249232-C-T

190370301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26249547-A-G

190370480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26249690-G-C

190370518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26249723-G-T

http://identifiers.org/hco/3/GRCh38#190370597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26249795-C-A

190370597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26249795-C-T

190370604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26249804-A-T

190371554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26250095-G-T

http://identifiers.org/hco/3/GRCh38#190371571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26250110-C-A

190372708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26250589-T-C

http://identifiers.org/hco/3/GRCh38#190372872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26250738-A-C

190373078-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26250893-A-T

190373118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26250933-A-G

190373141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26250955-G-A

190373351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26252130-T-C

190373414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26252197-T-C

190374003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26252747-T-A

190374124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26252864-G-C

190374168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26252906-C-G

190374288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26253044-T-C

190374298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26253054-T-A

http://identifiers.org/hco/3/GRCh38#190374367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26253169-A-C

190374367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26253169-A-G

190374441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26253259-G-A

190374441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26253259-G-T

190374461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26253279-G-A

190374461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26253279-G-T

190374599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26253422-T-C

190374634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26253455-A-T

http://identifiers.org/hco/3/GRCh38#190374778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26253546-C-A

190374778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26253546-C-T

190374787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26253557-C-T

190375200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26253969-A-G

190375200-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26253969-A-T

190375892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26255082-C-T

190376008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26255170-A-G

190376353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26255375-G-A

190376743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26255807-G-C

190376743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26255807-G-T

190376799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26255864-G-A

190377094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26256128-T-A

190377800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26258077-G-A

190377862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26258137-T-G

http://identifiers.org/hco/3/GRCh38#190377868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26258143-C-A

190377868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26258143-C-G

190377868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26258143-C-T

190378020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26258262-T-G

190378082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26258370-T-C

190378121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26258409-A-G

190378142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26258435-G-A

190378146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26258439-C-G

http://identifiers.org/hco/3/GRCh38#190378149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26258442-C-A

190378235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26258529-C-T

190378319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26258603-C-T

190378392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26258687-A-G

http://identifiers.org/hco/3/GRCh38#190378407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26258702-C-A

190378614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26258888-G-A

190378796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26259042-A-G

190378886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26259110-G-A

190379342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26259872-C-G

190379402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26259928-T-C

190379415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26259939-C-G

190379415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26259939-C-T

190379477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26260001-A-G

190379570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26260084-C-T

190379712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26260222-C-T

190379909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26260412-C-T

190380074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26260533-T-C

190380106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26260565-G-A

190380221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26260667-T-C

190380241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26260687-C-G

190380247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26260693-T-A

190380248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26260695-T-C

190380260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26260707-T-C

http://identifiers.org/hco/3/GRCh38#190380270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26260717-C-A

190380270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26260717-C-T

http://identifiers.org/hco/3/GRCh38#190381491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26263590-C-A

190381733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26263807-A-T

190381772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26263849-G-A

http://identifiers.org/hco/3/GRCh38#190381845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26263914-C-A

190381845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26263914-C-T

190383887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26266005-A-G

190384059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26266170-G-A

190384175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26266301-G-T

190384645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26266766-T-C

190384806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26266862-G-A

190384806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26266862-G-T

190384818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26266874-G-A

190384947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26267003-C-T

190385023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26272089-G-A

190385113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26272189-T-C

190385139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26272215-G-T

190385199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26272278-A-G

190385207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26272286-G-A

190385585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26272638-A-T

190385641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26272707-A-G

190385769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26272842-A-G

190386043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26273109-G-C

http://identifiers.org/hco/3/GRCh38#190386085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26273151-A-C

190387269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26275246-C-T

190387297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26275274-G-A

190387400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26275362-T-G

190387497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26281457-C-T

190387884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26281784-G-T

190387921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26281819-G-A

190387921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26281819-G-C

190387921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26281819-G-T

190387944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26281842-G-A

190387944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26281842-G-T

http://identifiers.org/hco/3/GRCh38#190387945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26281843-C-A

190387945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26281843-C-G

190387945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26281843-C-T

190388068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26281956-C-G

190388068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26281956-C-T

190388131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26282018-G-T

190388137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26282024-A-G

190388137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26282024-A-T

190388183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26282069-C-T

190388194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26282080-G-A

190388196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26282083-G-A

190388317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26282223-G-A

190388317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26282223-G-T

190388350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 26282256-C-T

190388407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 26282313-T-A

190388493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26282376-G-A

190388493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26282376-G-T

190388565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26282421-G-A

190388565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26282421-G-T

http://identifiers.org/hco/3/GRCh38#190388581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26282445-C-A

190388587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26282451-A-G

190388590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26282454-A-G

190388735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26282593-C-T

http://identifiers.org/hco/3/GRCh38#190388788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26282645-A-C

190388976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26282856-A-G

190389013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26282885-T-C

http://identifiers.org/hco/3/GRCh38#190389138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26283013-C-A

http://identifiers.org/hco/3/GRCh38#190389357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26283215-C-A

190389414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26283267-G-A

190389458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26283314-T-C

190389463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26283319-T-C

190389465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26283321-G-A

190389698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26283607-G-T

190389940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26283867-A-G

http://identifiers.org/hco/3/GRCh38#190390118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26284037-C-A

190391182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26285007-A-G

190391183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26285008-T-A

190391195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26285020-T-C

190391203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26285030-T-C

190391248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26285052-A-T

190391257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26285061-A-G

190391257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26285061-A-T

http://identifiers.org/hco/3/GRCh38#190391356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26285161-C-A

190391356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26285161-C-T

190391434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26285234-C-T

190391460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26285259-G-A

190391460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26285259-G-C

190391589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26285384-G-A

190391599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26285394-C-G

190391673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26285492-G-A

190391825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26285768-C-T

190391939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26285870-G-A

190391958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26285891-C-G

190392021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26285955-T-C

190392042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26285981-C-G

190392042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26285981-C-T

190392224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26286151-C-G

190392235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26286161-A-T

190392241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26286170-C-G

190392285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26286210-C-T

190392415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26286287-A-T

http://identifiers.org/hco/3/GRCh38#190392423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26286295-A-C

190392640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26286509-G-T

190392672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26286535-G-A

190392801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26286643-G-A

190392801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26286643-G-T

190392817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26286659-G-A

190392918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26286752-A-T

190393198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26287006-C-T

190394012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26287521-C-G

190394449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26287827-C-G

190394519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26287896-G-A

190394519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26287896-G-T

190394541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26287916-C-G

190394608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26287987-T-C

190394670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26288044-T-A

190394718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26288091-A-G

190395013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26288382-G-A

190395157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26288514-A-G

190395157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26288514-A-T

190395170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26288523-A-G

190395171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26288524-T-C

190396179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26288650-C-G

190396193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26288663-T-C

190396194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26288664-T-G

http://identifiers.org/hco/3/GRCh38#190396292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26288792-A-C

190396388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26288931-G-A

190396437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26288989-C-G

190396457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26289007-G-C

190396480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26289049-T-G

190396949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26289428-A-T

190397036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26289508-G-A

190397286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26289747-T-C

190397290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26289751-A-T

190397294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26289755-T-C

190397300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26289763-C-T

190397322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26289784-T-C

190398136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26290495-G-A

190398136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26290495-G-T

190398149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26290508-A-G

190398641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26290989-G-T

190398663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26291010-A-T

190398677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26291024-T-A

190401231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26291855-C-T

190401492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26292118-C-G

190401492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26292118-C-T

190401616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26292250-G-A

190401693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26292323-T-A

190402078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26292685-C-T

190402390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26292993-T-A

190402452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26293055-T-A

190402543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26293123-G-T

190402896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26293456-C-T

190402977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26293526-G-A

190402977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26293526-G-T

190402986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26293535-C-T

190403317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26293626-G-A

190403940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26294367-T-C

190404586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26296023-T-A

http://identifiers.org/hco/3/GRCh38#190404615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26296051-A-C

190404615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26296051-A-G

http://identifiers.org/hco/3/GRCh38#190404624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26296060-C-A

190404624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26296060-C-G

190404754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 26296235-T-G

190404847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26296328-C-T

190404865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26296346-T-G

190404873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26296354-C-T

190404930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26296411-C-T

190404934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 26296415-T-C

190407680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26297567-A-T

190407745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26297628-T-C

190408162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26299802-A-G

190408168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26299806-G-T

http://identifiers.org/hco/3/GRCh38#190408186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26299823-C-A

190408186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26299823-C-T

190408225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26299859-G-A

190408225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26299859-G-T

190408360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26299992-T-C

190408447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26300079-G-T

190408466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, missense_variant
orthologous variants: 26300098-G-T

190408525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26300156-G-A

190408525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26300156-G-T

http://identifiers.org/hco/3/GRCh38#190408546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26300174-A-C

http://identifiers.org/hco/3/GRCh38#190408578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26300206-C-A

190408598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26300207-T-C

190408598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26300207-T-G

190408652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26300263-G-A

190409226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26300700-G-A

190409405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26300859-A-G

190409484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron variant
orthologous variants: 26300892-T-C

190409896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 26301261-C-G

190409896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 26301261-C-T

190409960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 26301325-G-A

190409960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 26301325-G-T

190409973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 26301338-C-G

190409973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 26301338-C-T

190410139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: 26301511-T-G

http://identifiers.org/hco/3/GRCh38#190410251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26301582-C-A

190410267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: 26301598-T-C

190410285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: 26301616-G-A

190410285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: 26301616-G-T

190410358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: 26301686-G-T

190410362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: 26301690-C-T

190410427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: 26301756-C-T

190410462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: 26301791-T-C

190410476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: 26301797-G-T

http://identifiers.org/hco/3/GRCh38#190410489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26301810-A-C

190410577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: 26301897-A-G

190410580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: 26301900-A-G

http://identifiers.org/hco/3/GRCh38#190410595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26301915-C-A

190410612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: 26301932-G-T

190410739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: 26302055-T-C

190410746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: 26302062-T-C

http://identifiers.org/hco/3/GRCh38#190410904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26302214-A-C

http://identifiers.org/hco/3/GRCh38#190411382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26302394-C-A

190411382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: 26302394-C-G

190411452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: 26302464-A-G

190411527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: 26302511-A-G

190411700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: 26302673-C-T

190411702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: 26302675-G-C

http://identifiers.org/hco/3/GRCh38#190411721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#26302692-C-A

190411974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2037
most severe consequence: 3 prime UTR variant
orthologous variants: 26303750-G-T