http://identifiers.org/hco/18/GRCh38#32124888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21154094-C-A

32124888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21154094-C-T

http://identifiers.org/hco/18/GRCh38#32124927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21154135-A-C

32124958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21154165-A-G

32124998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21154198-G-A

32125133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21154506-T-G

32125173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21154540-T-C

32125183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21154550-A-G

32125328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21154823-G-T

32125457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21154923-T-G

32126118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21156914-G-C

http://identifiers.org/hco/18/GRCh38#32126351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21157145-A-C

32126351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21157145-A-G

32126481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21157272-T-C

http://identifiers.org/hco/18/GRCh38#32126903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21157657-C-A

32126903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21157657-C-G

http://identifiers.org/hco/18/GRCh38#32127373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21158015-A-C

http://identifiers.org/hco/18/GRCh38#32127742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21158338-C-A

32128238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21158645-G-A

32128238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21158645-G-T

32128595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21158705-T-C

http://identifiers.org/hco/18/GRCh38#32128993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21158941-A-C

32128993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21158941-A-G

32128993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21158941-A-T

http://identifiers.org/hco/18/GRCh38#32128998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21158973-C-A

32128998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21158973-C-G

32128998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21158973-C-T

32129037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21159063-A-G

32129037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21159063-A-T

32129078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21159101-G-A

32129078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21159101-G-T

32129145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21159169-A-G

32129192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21159216-T-C

32129213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21159237-G-A

32129213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21159237-G-C

32129213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21159237-G-T

http://identifiers.org/hco/18/GRCh38#32129220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21159245-C-A

32129220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21159245-C-T

32129460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21159466-G-A

32129460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21159466-G-T

32129474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21159480-G-A

32129474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21159480-G-C

32129474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21159480-G-T

http://identifiers.org/hco/18/GRCh38#32129476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21159482-A-C

32129476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21159482-A-T

32129892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21159868-G-A

32130515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21160393-A-G

32130522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21160400-A-G

32130565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21160439-A-G

32130798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21160669-A-G

32130825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21160689-T-C

32130831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21160695-C-T

32130928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21160802-C-T

32131270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21161005-T-C

32131270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21161005-T-G

32131277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21161012-G-A

32131277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21161012-G-T

32131423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21161138-A-T

32131526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21161247-T-C

32131605-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21161328-T-A

32132064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21162148-A-T

32156946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21170307-C-T

http://identifiers.org/hco/18/GRCh38#32157026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21170382-A-C

32157097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21170676-C-T

32157915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21171692-G-A

32158092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21171827-G-T

32159093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21172373-T-C

http://identifiers.org/hco/18/GRCh38#32159272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21172550-C-A

32160817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21172990-C-T

32160831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21173002-C-T

32160847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21173018-C-G

32160847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21173018-C-T

32160896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21173064-G-A

32161104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21173424-T-A

32161104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21173424-T-C

32162548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21177051-C-T

32162595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21177087-G-C

32162913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21177463-G-A

32162980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21177636-G-A

32168327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21185108-G-A

http://identifiers.org/hco/18/GRCh38#32185203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21202768-C-A

32185215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21202780-G-T

32185736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21203850-C-T

32185924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21204026-G-T

32188650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21204920-T-A

32189755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21205130-T-C

32190145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21205505-G-C

32190241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21205586-G-A

32190241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21205586-G-T

32190273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21205618-T-C

32190358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21205707-C-T

32190798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21206138-C-T

32191186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21206541-A-G

32191186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21206541-A-T

32191285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21207117-T-C

32191501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21207293-G-A

32191501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21207293-G-C

32191804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21207960-T-C

32191914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21208102-T-C

http://identifiers.org/hco/18/GRCh38#32191937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21208125-A-C

http://identifiers.org/hco/18/GRCh38#32192656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21208724-C-A

32192656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21208724-C-T

32192698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21208766-G-C

32192698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21208766-G-T

32192736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21209364-T-C

http://identifiers.org/hco/18/GRCh38#32192855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21209473-C-A

http://identifiers.org/hco/18/GRCh38#32192858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21209476-C-A

32192858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21209476-C-T

http://identifiers.org/hco/18/GRCh38#32192865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21209481-C-A

http://identifiers.org/hco/18/GRCh38#32192880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21209495-C-A

http://identifiers.org/hco/18/GRCh38#32192895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21209506-C-A

32192895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21209506-C-T

32192925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21209536-C-G

http://identifiers.org/hco/18/GRCh38#32192958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21209567-C-A

32192958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21209567-C-T

http://identifiers.org/hco/18/GRCh38#32192974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21209583-C-A

32192974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21209583-C-T

32193029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21209639-G-A

32193253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21210594-G-A

32193557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21211251-T-C

32193649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21211335-C-T

32195132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21213236-C-T

http://identifiers.org/hco/18/GRCh38#32195306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21213391-C-A

32195306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21213391-C-G

32195400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21213480-T-C

32201031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21216848-T-C

32201129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21216960-G-A

32201201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21217015-A-G

http://identifiers.org/hco/18/GRCh38#32203019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21217262-C-A

32203019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21217262-C-T

http://identifiers.org/hco/18/GRCh38#32203092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21217320-C-A

32203176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21217400-A-G

32204238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21219275-C-T

http://identifiers.org/hco/18/GRCh38#32204281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21219318-C-A

32204281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, missense_variant
orthologous variants: 21219318-C-G

32204281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21219318-C-T

32204357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, missense_variant
orthologous variants: 21219394-T-C

32205781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21219642-T-C

32205923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21219814-G-A

32206652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21221036-C-T

32207075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21221421-G-A

32207139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21221481-T-C

32207166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21221516-T-C

32207166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21221516-T-G

http://identifiers.org/hco/18/GRCh38#32207185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21221535-C-A

32207185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21221535-C-G

32207185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21221535-C-T

32207196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21221544-G-A

32207196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21221544-G-T

http://identifiers.org/hco/18/GRCh38#32207230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21221578-A-C

32207370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21221720-G-A

32207397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, missense_variant
orthologous variants: 21221747-T-G

32207451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, missense_variant
orthologous variants: 21221801-G-C

32207703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21222023-T-C

32207793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21222111-T-C

32207841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21222158-G-A

32207858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21222175-T-C

32207981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21222251-A-G

32207981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21222251-A-T

32208058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21222315-T-C

32208067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21222327-C-T

32208353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21222599-T-G

http://identifiers.org/hco/18/GRCh38#32208517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21222687-C-A

32208517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21222687-C-T

32208549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21222698-G-A

32208568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21222719-G-A

32208763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21222939-C-T

32208995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21223133-G-C

32209008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21223155-A-G

32209141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21223287-C-T

32210479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21224106-C-T

32210481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21224107-A-G

32210481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21224107-A-T

32210601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21224231-C-T

32210640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21224270-T-C

32210722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21224352-A-G

32210743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21224373-G-C

http://identifiers.org/hco/18/GRCh38#32210765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21224395-A-C

32210765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21224395-A-G

32210808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21224415-G-A

32210891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21224487-G-C

32211322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21224782-T-C

32211434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21224888-C-G

32212971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21226006-T-C

32213002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21226101-G-A

32213002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21226101-G-T

http://identifiers.org/hco/18/GRCh38#32213029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21226200-C-A

32213029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21226200-C-G

32213071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21226247-G-T

32213177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21226339-A-G

32213180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21226342-G-A

32213180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21226342-G-T

32213219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21226381-T-C

32213219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21226381-T-G

32213222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21226384-T-A

32213271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, missense_variant
orthologous variants: 21226433-A-G

32213441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21226603-A-G

http://identifiers.org/hco/18/GRCh38#32213603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21226766-C-A

32213603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21226766-C-G

32213955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21227076-T-C

32214111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21227220-A-G

http://identifiers.org/hco/18/GRCh38#32214284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21227363-A-C

32214284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21227363-A-T

32214931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21227835-G-A

32214931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21227835-G-T

32214933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21227837-G-A

32214933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21227837-G-T

http://identifiers.org/hco/18/GRCh38#32215029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21227928-C-A

32215095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21227994-T-C

32215128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21228027-G-A

32215166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, missense_variant
orthologous variants: 21228065-G-A

32215266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21228165-G-A

32215301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21228194-T-A

32217030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, missense_variant
orthologous variants: 21229220-C-T

32217038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, missense_variant
orthologous variants: 21229237-A-G

32217066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, missense_variant
orthologous variants: 21229267-C-T

32217289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21229897-A-G

32217429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21230047-C-T

32217438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21230053-C-G

32217572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21230164-T-A

32217851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21230435-T-C

32217878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21230462-G-C

http://identifiers.org/hco/18/GRCh38#32217909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21230493-A-C

32217986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21230570-G-T

32218016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21230585-T-C

http://identifiers.org/hco/18/GRCh38#32218058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21230658-C-A

32218058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21230658-C-T

http://identifiers.org/hco/18/GRCh38#32218089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21230817-C-A

32218089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21230817-C-T

32218148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21230876-G-T

32218153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21230881-T-G

32218687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21231303-C-G

32218738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21231351-T-C

32218753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21231366-G-A

32219563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21232480-G-A

32220060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21232942-G-A

32220096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21232978-T-C

32220133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21233014-G-A

32220133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21233014-G-C

32220133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21233014-G-T

32220264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21233127-G-A

32220671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21233510-T-C

32234565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21234075-T-C

32234838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21234261-T-C

32235325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21236141-T-C

32235325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21236141-T-G

32235330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21236146-A-G

http://identifiers.org/hco/18/GRCh38#32235380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21236196-C-A

http://identifiers.org/hco/18/GRCh38#32235446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21236272-C-A

32235952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21236782-T-G

32236011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21236843-T-C

32236702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21237964-T-A

32236915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21238179-A-G

http://identifiers.org/hco/18/GRCh38#32238579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21239113-C-A

32238607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21239141-C-T

32238664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21239227-T-C

32238871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21239411-T-C

32239106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21239627-C-T

32244830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21242846-G-A

32244830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21242846-G-T

32244858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21242874-T-C

32244982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21242992-T-A

32244982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21242992-T-C

http://identifiers.org/hco/18/GRCh38#32244988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21242998-A-C

32245290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21243305-C-T

32245362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21243373-T-C

32246256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21244596-G-A

32249210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21247198-A-G

32249233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21247211-T-C

32249412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21247395-G-A

32249539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21247506-T-C

32249588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21247555-C-T

32250052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21248020-T-A

32250052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21248020-T-G

32250080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21248048-T-C

32251507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21249208-C-G

32251507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21249208-C-T

http://identifiers.org/hco/18/GRCh38#32251556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21249261-C-A

32251556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21249261-C-T

32251792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21249485-T-G

32252364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21251142-G-A

32252364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21251142-G-C

32252364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21251142-G-T

32252368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21251146-G-T

32252373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21251151-T-G

32252409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21251186-A-G

32252452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21251229-T-A

32255132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21251655-T-C

32255215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21251738-A-G

32255463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21252221-G-C

32255477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21252235-A-G

32255618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21252373-G-A

32255789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21252526-G-A

32257977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21253567-A-G

32257977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21253567-A-T

32258030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21253620-T-C

32258067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21253657-C-T

32258131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21253716-A-G

http://identifiers.org/hco/18/GRCh38#32258368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21253923-C-A

32258368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21253923-C-G

32258471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21254026-T-C

32258788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21254305-G-A

http://identifiers.org/hco/18/GRCh38#32261003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21255074-C-A

32261155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21255189-G-A

32261155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21255189-G-T

32261171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21255205-C-T

32261253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21255276-G-A

32261443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21256143-C-T

32261548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21256260-T-C

32261661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21256362-A-G

32261693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21256388-G-T

32261739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21256431-C-G

32261915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21256557-T-G

32262077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21256746-G-A

32262077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21256746-G-T

32262173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21256928-C-T

32262352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21257065-G-A

32262362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21257075-T-G

32262780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21257389-T-C

32262873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21257457-T-C

32262903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21257487-A-G

32262952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21257519-A-G

32263239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21257706-T-A

32263239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21257706-T-C

32263239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21257706-T-G

32263241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21257708-T-C

32263241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21257708-T-G

32263328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21257744-G-T

32263413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21257818-G-T

32263414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21257819-C-T

32263651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21258055-A-G

http://identifiers.org/hco/18/GRCh38#32263743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21258141-C-A

32263788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21258255-A-G

32264099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21258580-G-A

32264131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21258612-A-G

32264223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21258695-A-G

32264388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21258845-G-A

32264390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21258847-A-G

32264683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21259131-G-C

32264706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21259158-T-C

32264922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21259400-T-G

32264979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21259455-G-C

32264979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21259455-G-T

http://identifiers.org/hco/18/GRCh38#32265014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21259463-C-A

32265119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21259529-G-T

32265251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21259647-G-A

32265258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21259654-A-G

http://identifiers.org/hco/18/GRCh38#32265335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21259705-C-A

32265389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21259792-T-C

32265414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21259806-C-G

http://identifiers.org/hco/18/GRCh38#32265425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21259817-C-A

32265515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21259898-G-A

32265572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21259969-A-G

32265575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21259976-A-G

32265592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21259991-C-T

http://identifiers.org/hco/18/GRCh38#32265760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21260153-C-A

32265828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21260221-A-G

32265933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21260329-T-C

http://identifiers.org/hco/18/GRCh38#32265964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21260357-A-C

http://identifiers.org/hco/18/GRCh38#32266214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21260598-C-A

32266304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21260669-T-C

32266375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21260739-C-G

32266375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21260739-C-T

http://identifiers.org/hco/18/GRCh38#32266439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21260807-C-A

http://identifiers.org/hco/18/GRCh38#32266447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21260815-C-A

32266507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21260871-T-C

32266519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21260883-G-C

32266699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21261074-T-C

32266750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21261123-T-C

32266750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21261123-T-G

32266753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21261126-G-T

32266800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21261172-C-T

32266811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21261183-C-G

http://identifiers.org/hco/18/GRCh38#32267053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21261396-C-A

32267117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21261459-G-A

32267117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21261459-G-T

32267189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21261523-T-G

32267483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21261806-G-A

32267484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21261807-G-T

32267809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21262123-G-T

http://identifiers.org/hco/18/GRCh38#32267824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21262138-C-A

32267824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21262138-C-T

32267826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21262140-C-T

32267973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21262284-A-G

32267988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21262299-A-G

32268017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, missense_variant
orthologous variants: 21262328-C-T

32268029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21262340-A-G

32268099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21262410-T-C

32268102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21262413-G-A

32268204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21262515-C-T

32268342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21262653-C-G

32268342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21262653-C-T

32268365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, missense_variant
orthologous variants: 21262676-C-G

32268365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, missense_variant
orthologous variants: 21262676-C-T

http://identifiers.org/hco/18/GRCh38#32268508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21262822-C-A

32268534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, missense_variant
orthologous variants: 21262848-C-G

32268609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21262923-T-C

32268766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, missense_variant, splice_acceptor_variant, splice_region_variant
orthologous variants: 21263080-C-T

32268890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21263319-T-C

32268890-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21263319-T-G

32269159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21263572-C-T

32269170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21263582-C-T

32269177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21263587-G-A

32270026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, missense_variant
orthologous variants: 21264225-G-A

http://identifiers.org/hco/18/GRCh38#32270070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21264269-C-A

32270070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21264269-C-T

32270076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21264275-G-A

32270076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21264275-G-T

32270114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21264313-C-T

32270163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21264347-T-A

32270163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21264347-T-C

32270210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 21264383-G-A

32270210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 21264383-G-C

32270300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21264473-A-G

32270304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, missense_variant
orthologous variants: 21264477-A-T

32270367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, missense_variant
orthologous variants: 21264540-C-T

32270386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 21264559-G-A

http://identifiers.org/hco/18/GRCh38#32270690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21264938-A-C

32270905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21265078-T-C

32271569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21265682-G-C

32271633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21265752-A-T

32271704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21265819-T-C

32271855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21265965-G-C

32271999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21266087-C-G

32272083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21266154-C-T

http://identifiers.org/hco/18/GRCh38#32272183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21266244-A-C

http://identifiers.org/hco/18/GRCh38#32272235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21266292-A-C

32273394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21268176-T-C

32273835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21268449-T-C

32273838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21268452-T-C

32273902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21268477-C-G

32274016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21268571-T-C

32274159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21268698-T-C

32274229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21268774-C-T

32274258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21268807-T-C

32274258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21268807-T-G

32274916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21269432-C-T

32274935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21269451-G-A

32275051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21269589-T-G

32275256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21269719-G-A

32276091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21270109-G-A

32276202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21270208-A-G

32276202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21270208-A-T

32276264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21270257-G-A

32276304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21270299-T-C

32276586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21270547-C-T

http://identifiers.org/hco/18/GRCh38#32276715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21270691-C-A

32276789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21270769-C-T

32276811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21270791-G-T

32276957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21270891-T-C

32277197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21271137-T-C

32277488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21271421-A-G

32277600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21271516-C-T

32277623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21271539-T-G

32278071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21271743-G-C

http://identifiers.org/hco/18/GRCh38#32278084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21271756-A-C

32278123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21271790-G-A

32278779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21272416-A-G

32279075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21272681-T-C

32280309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21273959-G-A

32280552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21274124-T-C

http://identifiers.org/hco/18/GRCh38#32280593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21274166-A-C

32280594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21274167-G-A

32280847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21274370-T-G

32281193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21274848-A-G

32281475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21275288-T-C

32281518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21275330-C-T

http://identifiers.org/hco/18/GRCh38#32281580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21275387-C-A

32282543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21275563-T-C

32282995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21276538-T-A

32284003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21277507-C-T

32284078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21277572-C-T

32284152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21277651-C-T

32284309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21277850-C-G

32284309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21277850-C-T

32284494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21278784-G-A

32284494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21278784-G-C

32284496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21278786-G-C

http://identifiers.org/hco/18/GRCh38#32284650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21278934-A-C

32284650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21278934-A-G

32285216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21279189-T-C

32285376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21279338-C-T

32285388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21279349-C-T

32285394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21279355-C-T

32285710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21279630-A-G

32285800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21279687-T-G

32285996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21279912-A-G

32286034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21279941-A-G

32286068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21279986-C-T

http://identifiers.org/hco/18/GRCh38#32286366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21280102-C-A

32286366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21280102-C-T

32286580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21280286-T-C

http://identifiers.org/hco/18/GRCh38#32286651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21280357-C-A

32286666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21280372-A-G

32286892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21280583-A-T

32286905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21280596-T-C

32286942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21280634-G-A

32286942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21280634-G-C

32286942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21280634-G-T

32286962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21280664-T-A

http://identifiers.org/hco/18/GRCh38#32287005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21280759-C-A

32287005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21280759-C-G

32287005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21280759-C-T

32287203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: missense variant
orthologous variants: 21280961-T-C

32287346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: synonymous variant
orthologous variants: 21281104-A-T

32287439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21281197-G-A

32287439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21281197-G-C

32287443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21281201-C-T

32287475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21281233-G-A

32287516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21281274-G-A

32287529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21281287-G-A

http://identifiers.org/hco/18/GRCh38#32287865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21281623-C-A

32287865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21281623-C-G

32287865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21281623-C-T

32287924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21281682-G-A

32287924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21281682-G-T

32287997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21281755-A-G

32287997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 21281755-A-T

http://identifiers.org/hco/18/GRCh38#32295324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21288598-C-A

32295331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21288605-A-G

32295660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21288901-T-C

32295805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21289040-G-A

32296920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21289730-T-G

32296970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21289795-T-C

32297159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21289951-C-T

32297207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21289983-A-G

32297220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21289996-C-T

32297221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21289997-C-T

32297244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21290020-A-G

32297252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21290028-C-T

http://identifiers.org/hco/18/GRCh38#32297355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21290117-C-A

32297357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21290119-T-A

32297419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21290174-T-A

32297419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21290174-T-C

32298052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21290933-T-C

32298195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21291065-A-G

32298795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21291745-T-C

32299165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21292172-G-A

32299996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21292600-G-C

32300376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21292933-C-T

32302466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21293487-T-C

http://identifiers.org/hco/18/GRCh38#32303049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21294995-C-A

32303049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21294995-C-G

32303152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21295077-A-G

32303289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21295201-C-T

32303340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21295252-T-C

32303345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21295257-T-C

32303643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21295545-C-T

32306939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21297935-G-A

32307294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21298816-C-T

32308045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21299214-C-G

32308045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21299214-C-T

32308222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21299387-T-G

32308734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21300507-C-T

32308888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21300646-T-G

32309020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21300748-C-T

32309144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21300872-C-T

32310050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21301665-A-G

32310050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21301665-A-T

32310060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21301671-G-C

32310060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21301671-G-T

http://identifiers.org/hco/18/GRCh38#32310096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21301709-C-A

32310096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21301709-C-G

32310130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21301742-C-T

http://identifiers.org/hco/18/GRCh38#32310131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21301743-C-A

32310175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21301779-T-C

32310336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21301936-A-G

32310365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21301964-C-T

http://identifiers.org/hco/18/GRCh38#32310401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21301999-C-A

32310401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21301999-C-T

http://identifiers.org/hco/18/GRCh38#32310413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21302011-C-A

32310413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21302011-C-T

http://identifiers.org/hco/18/GRCh38#32310433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21302030-C-A

32310433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21302030-C-T

http://identifiers.org/hco/18/GRCh38#32310438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21302035-C-A

32310438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21302035-C-T

32310468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21302063-G-A

32310468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21302063-G-T

32314898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21303216-T-A

32315029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21303334-G-C

32317450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21304954-G-A

32317506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21305009-T-C

32317550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21305048-C-T

32317571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21305069-T-C

32317619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21305117-A-T

32317787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21305265-G-A

32317832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21305309-G-C

32318339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21305821-G-A

32318500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21305989-C-G

32318566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21306042-T-C

32318566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21306042-T-G

32318618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21306114-C-G

32318618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21306114-C-T

32318771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21306257-G-A

32319104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21306566-T-C

32319104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21306566-T-G

32319458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21307068-C-G

32319872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21307271-T-C

http://identifiers.org/hco/18/GRCh38#32319921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21307318-C-A

32319947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21307344-C-T

32320225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21307585-T-A

http://identifiers.org/hco/18/GRCh38#32320232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21307592-C-A

32320781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21308682-T-C

32320962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21308906-G-A

32321151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21309085-T-C

http://identifiers.org/hco/18/GRCh38#32321172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21309104-A-C

32321176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21309108-T-C

32323729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21310017-A-T

32323801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21310103-T-C

32323900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21310199-C-T

32324318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21310586-C-T

32325442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21311305-A-G

32325603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21311405-T-C

32325683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21311465-C-T

32325702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21311484-C-T

32326065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21311822-A-G

http://identifiers.org/hco/18/GRCh38#32326277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21312029-C-A

32326277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21312029-C-T

32326587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21312619-T-C

32326587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21312619-T-G

32326657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21312708-C-G

32327117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21313275-T-C

32330716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21314321-T-A

32330734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21314339-T-G

32330982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21314569-G-A

32331601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21314982-G-A

32331601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21314982-G-T

http://identifiers.org/hco/18/GRCh38#32331615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21314998-C-A

32331615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21314998-C-T

http://identifiers.org/hco/18/GRCh38#32331709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21315095-C-A

32331776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21315154-G-C

32331776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21315154-G-T

32331784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21315163-A-G

32331808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21315186-T-C

32331808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21315186-T-G

32333080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21315309-G-C

http://identifiers.org/hco/18/GRCh38#32333091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21315311-A-C

32333132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21315350-T-G

32333153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21315365-G-A

32333159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21315371-G-A

32333170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21315383-G-C

32333201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21315419-T-A

32333201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21315419-T-G

32333220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21315442-G-A

http://identifiers.org/hco/18/GRCh38#32333301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21315500-A-C

32333967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21317408-C-T

32334144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21317584-A-G

32334245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21317684-T-C

32334321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21317760-C-T

32334521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21317988-G-C

32334541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21318008-G-A

32334667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21318140-T-C

32334884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21318379-T-C

32335818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21319310-A-G

32335943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21319434-C-T

32335955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21319446-T-C

32335955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21319446-T-G

32336810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21320587-G-A

32337059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21320843-T-C

32337487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21321288-C-G

32337553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21321352-T-C

32337558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21321357-A-G

32337966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21321759-T-C

32339862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21322055-C-T

32339969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21322202-C-T

http://identifiers.org/hco/18/GRCh38#32342855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21322510-C-A

32342906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21322564-T-G

32343792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21323245-T-C

32343904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21323358-C-T

32344603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21323966-T-C

32344727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21324086-A-G

32345221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21324219-A-G

32345502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21324457-A-T

32346465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21325125-T-C

32346605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21325255-G-A

32346645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21325305-T-C

32347572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21325963-G-A

32347630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21325999-G-C

32347823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21326172-T-C

32348130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21326579-A-G

http://identifiers.org/hco/18/GRCh38#32348216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21326667-C-A

32348353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21326807-C-T

32348951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21327084-G-A

http://identifiers.org/hco/18/GRCh38#32349537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21328642-C-A

32350015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21329107-G-A

http://identifiers.org/hco/18/GRCh38#32350063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21329155-A-C

32350065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21329157-C-T

32350089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21329172-C-T

32350463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21329570-G-A

32350583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21329685-C-T

32351129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21330638-A-G

http://identifiers.org/hco/18/GRCh38#32351693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21331149-C-A

32351716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21331181-A-T

32351725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21331190-G-A

32351725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21331190-G-T

32351752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21331218-G-T

32352291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21331713-G-C

32352759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21332049-A-G

32352759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21332049-A-T

32352981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21332242-T-C

32353098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21332396-T-C

32353290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21332639-G-A

32353290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21332639-G-C

32353290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21332639-G-T

32353598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21333169-T-A

32353598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21333169-T-C

32353863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21333402-G-A

32353983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21333525-C-T

32354007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21333550-G-A

32354044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21333586-A-G

32354063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21333604-T-C

32354127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21333668-T-C

32354135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21333676-G-A

32354135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21333676-G-C

32354691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21334169-G-T

32354784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21334413-T-C

32355423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21334835-A-G

32355663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21335161-T-C

http://identifiers.org/hco/18/GRCh38#32355706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21335217-C-A

32355806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21335314-A-G

32356107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21335616-A-T

32356138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21335635-T-C

32356138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21335635-T-G

32356354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21335811-A-T

32356387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21335848-G-A

32356498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21335927-T-C

32356534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21335963-G-A

32356933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21336269-T-C

32357550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21336917-T-C

32358079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21337335-C-T

http://identifiers.org/hco/18/GRCh38#32358121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21337383-C-A

32358121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21337383-C-T

32358296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 21337578-G-A

32358296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 21337578-G-T

http://identifiers.org/hco/18/GRCh38#32358652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21337899-C-A

32359014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21338151-T-A

32360208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21340390-G-A

32360299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21340468-A-T

32360403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21340567-C-T

32360673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21340784-G-C

32361680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21340875-C-T

32361793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21340986-G-T

32361965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21341127-A-G

32362077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21341224-C-T

32362105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21341259-C-G

32362105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21341259-C-T

32362549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21342248-T-C

http://identifiers.org/hco/18/GRCh38#32362644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21342338-C-A

32362644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21342338-C-T

32363184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21342821-G-A

32366139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21343866-C-G

32366839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21344483-C-G

32366839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21344483-C-T

32366954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21344584-T-C

32367161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21344867-C-G

32367275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21345016-T-C

32367307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21345052-G-A

32367351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21345121-C-T

32368872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21345702-G-A

32368872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21345702-G-T

http://identifiers.org/hco/18/GRCh38#32370840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21346749-C-A

32370840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21346749-C-T

32370937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21346844-C-T

http://identifiers.org/hco/18/GRCh38#32371078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21346973-A-C

32371166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21347037-C-T

http://identifiers.org/hco/18/GRCh38#32371213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21347118-C-A

http://identifiers.org/hco/18/GRCh38#32371327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21347228-A-C

32371327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21347228-A-G

32371493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21347366-G-A

http://identifiers.org/hco/18/GRCh38#32371847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21347714-A-C

32371907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21347749-G-T

32372089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21347878-C-T

32372194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21347987-C-T

32372331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21348109-A-T

32372686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21348460-G-C

32372792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21348564-G-C

32373403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21349206-T-C

32373798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21350049-T-C

32373840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21350094-A-T

32374059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21350709-C-T

32374060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21350710-G-A

32374060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21350710-G-C

32374388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21351032-A-G

32374415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21351059-G-A

32374774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21351395-T-C

32374782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21351403-G-A

32374782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21351403-G-C

32374941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21351559-C-T

32374998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21351649-C-T

32378785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21353239-G-T

32378836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21353298-C-T

32379038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21353470-G-A

32379038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21353470-G-T

32379136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21353555-A-G

32379310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21353693-T-C

http://identifiers.org/hco/18/GRCh38#32379358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21353741-C-A

32379508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21353766-C-T

32380059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21354136-A-T

32381037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21355230-A-G

32381233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21355408-C-T

32381445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21355929-A-G

32381455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21355939-G-A

32381898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21356386-C-T

32382021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21356514-C-T

32382445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21357086-C-T

32382459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21357100-G-A

32382812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21357323-C-T

http://identifiers.org/hco/18/GRCh38#32382884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21357383-C-A

32383211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21357682-A-G

32383215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21357686-G-A

32383493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21357919-G-A

32383758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21358175-A-G

http://identifiers.org/hco/18/GRCh38#32383909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21358609-A-C

32384000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21358705-T-C

http://identifiers.org/hco/18/GRCh38#32384010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21358715-C-A

32384760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21358952-T-G

http://identifiers.org/hco/18/GRCh38#32385113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21359922-C-A

32385314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21360041-T-C

32385628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21360328-A-T

32385630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21360330-G-C

32385653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21360336-C-T

32385770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21360461-C-T

32385832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21360524-C-T

32386038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21360715-T-C

32386163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21360835-C-T

32386369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21361039-C-G

32386369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21361039-C-T

32386376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21361045-T-C

32386464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21361133-T-C

32386563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21361231-C-T

32386565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21361233-C-T

32386566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21361234-G-A

32386661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21361305-G-A

32386707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21361351-G-A

http://identifiers.org/hco/18/GRCh38#32386721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#21361365-C-A

32387044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21362238-T-G

32387265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21362455-A-G

32387282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21362476-G-A

32387342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21362531-T-C

32388162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21363408-T-C

32388162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21363408-T-G

32388228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21363444-T-A

http://identifiers.org/hco/18/GRCh38#32388355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21363548-C-A

32388406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21363597-T-C

32388795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21363993-A-G

32388973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21364157-A-G

32389029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21364219-C-T

32389040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21364230-G-A

32389043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21364233-T-A

32389051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21364241-T-C

32389280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21365180-C-T

32389307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21365205-C-T

32389387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21365276-T-C

32389396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21365285-C-G

32389396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21365285-C-T

32389452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21365323-G-A

32389487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21365339-C-T

32389566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21365407-A-G

http://identifiers.org/hco/18/GRCh38#32389659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21365514-A-C

32389814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21365673-C-T

32391157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21367483-C-T

32391250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21367556-G-A

http://identifiers.org/hco/18/GRCh38#32391481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21367756-A-C

32391592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21367841-T-G

32391737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21367984-C-T

32391751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21368000-T-C

32391787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21368039-T-C

32391852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21368106-G-A

32391922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21368168-A-G

32392041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21368244-G-T

32392091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21368294-T-C

32392323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21368506-A-G

32392378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21368561-C-T

32392391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21368574-A-G

32392395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21368578-T-A

32392531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21368713-T-G

32392751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21368906-T-C

32392751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21368906-T-G

32392768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21368927-A-T

http://identifiers.org/hco/18/GRCh38#32392801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21368961-C-A

32392801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21368961-C-G

32392821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21368981-T-C

32392889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21369052-T-C

http://identifiers.org/hco/18/GRCh38#32393019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21369182-C-A

32393019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 21369182-C-G

32393019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 21369182-C-T

http://identifiers.org/hco/18/GRCh38#32393031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21369194-C-A

32393054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21369217-T-A

32393054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21369217-T-C

32393068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21369231-A-G

http://identifiers.org/hco/18/GRCh38#32393108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21369270-C-A

32393126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21369366-T-A

32393126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21369366-T-G

32393204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21369585-G-T

http://identifiers.org/hco/18/GRCh38#32393224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21369629-C-A

32393224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21369629-C-T

32393284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21369789-T-C

32393317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21369822-G-T

32393455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21369938-A-T

32393472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21369959-T-C

32393663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21370152-C-T

32393839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21370331-C-T

32394044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21370551-T-G

http://identifiers.org/hco/18/GRCh38#32394068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21370574-A-C

32394706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21370886-G-A

32394735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21370915-G-A

32394806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21370963-T-C

32395051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21371204-T-A

32395171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21371302-C-T

32395257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21371387-C-T

32395442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21371551-G-C

32395445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21371554-G-A

32395518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21371633-A-T

32395646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21371889-G-A

32401532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21372481-T-C

32401586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21372534-G-A

32402249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21373166-G-A

32402261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21373178-T-C

32402289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21373206-T-C

32402312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21373219-A-G

32402544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21373451-T-G

32402678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21373571-A-G

32402735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21373627-T-C

32402763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21373657-C-T

32403532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21374068-C-T

32403765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21374168-A-G

32403798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21374201-A-G

32403854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21374248-T-C

32404052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21374644-G-A

32404158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21374725-T-C

32404232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21374785-C-T

32404546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21375426-G-A

32404546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21375426-G-T

32404716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21375572-T-C

32404797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21375649-G-A

32405561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21375787-T-C

32405683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21375909-T-A

32405893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21376066-C-G

32405923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21376101-T-A

32405959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21376137-A-G

32406274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21376399-C-T

32406440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21376547-C-T

32406444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21376551-C-T

32406695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21376768-G-A

32406811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21376862-T-G

32407102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21377137-C-T

32408719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21378910-C-T

32408906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21379084-G-A

32409089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21379259-T-C

32409182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21379353-A-G

32409188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21379359-G-A

http://identifiers.org/hco/18/GRCh38#32409221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21379393-A-C

32409424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21379588-T-C

32409518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21379661-A-G

32409741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21379878-T-C

32409831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21379970-A-T

32409988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21380108-T-C

32410082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21380437-C-T

32410084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21380439-C-G

32410186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21380528-G-A

http://identifiers.org/hco/18/GRCh38#32413310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21381888-C-A

32413349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21381926-G-C

32413458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21382042-A-G

32413548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21382135-C-T

32414036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21382828-A-G

32418985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21383465-C-T

32419310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21383752-A-G

32419470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21383891-C-G

32419470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21383891-C-T

32419552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21383973-G-A

http://identifiers.org/hco/18/GRCh38#32419580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21384001-A-C

32419623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21384043-G-A

32419714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21384166-A-G

32420149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21384626-C-G

32420157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21384634-T-C

http://identifiers.org/hco/18/GRCh38#32420274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21384755-C-A

32420274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21384755-C-T

32420303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21384781-G-C

32420329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21384800-T-C

http://identifiers.org/hco/18/GRCh38#32420470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21384923-C-A

32421696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21385483-G-A

32422435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21386335-A-G

32422681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21386559-C-T

http://identifiers.org/hco/18/GRCh38#32422687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21386564-C-A

32423039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21386860-A-G

32423092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21386909-G-T

32423299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21387099-T-C

http://identifiers.org/hco/18/GRCh38#32424334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21387809-C-A

32424334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21387809-C-T

32424458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21387920-G-A

32424711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21388143-G-A

32424812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21388244-T-C

32425239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21388665-T-C

32425548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21388955-G-A

32425548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21388955-G-C

32425669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21389209-T-G

32425837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21389340-C-T

32425969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21389428-A-G

32426631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21389854-C-T

32427056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21389893-T-C

32427305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21390139-G-A

32427419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21390254-G-C

32427831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21390568-A-T

32427874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21390611-G-A

32428041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21390761-A-G

http://identifiers.org/hco/18/GRCh38#32428270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21390983-C-A

32428270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21390983-C-T

32429350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21392159-C-T

32429422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21392237-T-C

32429483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21392294-A-G

32429643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21392451-A-G

http://identifiers.org/hco/18/GRCh38#32429662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21392468-C-A

32429662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21392468-C-T

32429791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21392600-C-T

32429930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21392729-G-A

32429930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21392729-G-T

32429995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21392794-G-A

http://identifiers.org/hco/18/GRCh38#32430023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21392847-A-C

32430023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21392847-A-G

32430092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21393028-G-A

32430110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21393046-G-T

32430189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21393118-T-C

32430588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21393515-A-G

32430703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21393613-A-G

http://identifiers.org/hco/18/GRCh38#32430809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21393782-C-A

32431132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21394105-C-T

32436480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21402457-A-T

32436502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21402480-T-C

32436518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21402496-C-G

32436533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21402510-T-C

http://identifiers.org/hco/18/GRCh38#32436646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21402612-C-A

32436656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21402622-C-T

32436870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21403285-T-C

32436905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21403322-A-G

32437532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21403841-C-T

32437707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21404007-C-T

32438198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21404639-A-G

32438236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21404667-G-A

http://identifiers.org/hco/18/GRCh38#32438381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21404786-C-A

32438426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21404814-C-T

32438432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21404826-G-A

32438710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21405091-T-C

32438728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21405107-T-C

32439474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21405633-G-A

32439592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21405729-T-A

32441418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21405804-G-C

32441539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21405921-T-A

32441539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21405921-T-G

32441786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21406168-T-G

http://identifiers.org/hco/18/GRCh38#32442378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21406752-C-A

32442443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21406819-C-G

32442452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21406827-T-C

32442523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21406898-C-T

32442647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21406987-T-A

32442653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21406992-C-T

http://identifiers.org/hco/18/GRCh38#32442680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21407019-C-A

http://identifiers.org/hco/18/GRCh38#32442701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21407037-A-C

32442714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21407050-T-A

32442747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21407082-G-C

32442792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21407127-T-C

32442829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21407164-A-G

32442833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21407168-A-G

32443052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21407375-T-A

32443052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21407375-T-C

32443163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21407489-A-G

http://identifiers.org/hco/18/GRCh38#32443276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21407593-A-C

32443360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21407685-T-A

32443360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21407685-T-C

32443360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21407685-T-G

32443570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21407877-A-G

http://identifiers.org/hco/18/GRCh38#32443649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21407951-C-A

32443827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21408123-A-G

32444666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21408446-T-C

32444669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21408449-C-T

32445066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21408866-G-C

32445122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21408919-G-T

32445219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21409008-A-G

32445298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21409079-T-C

32445396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21409328-T-C

http://identifiers.org/hco/18/GRCh38#32445425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21409414-C-A

32445458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21409447-T-A

32445494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21409478-T-C

32445556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21409543-T-C

32446052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21409982-A-G

32446472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21410399-T-C

32446577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21410503-G-A

32446870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21410715-A-G

32446991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21410822-C-T

http://identifiers.org/hco/18/GRCh38#32447044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21410872-A-C

32447063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21410891-G-C

32447080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21410906-A-G

32447289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21411095-T-C

32447619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21411528-C-G

32447763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21411689-T-C

32447861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21411766-T-C

32447928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21411813-T-C

32448528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21412983-T-C

32448541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21412996-T-C

32448570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21413022-C-T

32448681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21413133-T-C

32448862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21413301-C-T

32449070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21413517-C-T

http://identifiers.org/hco/18/GRCh38#32449261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21413696-C-A

32449884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21414871-C-T

32449909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21414896-A-G

32450048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21415034-C-G

32450087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21415073-C-T

32450096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21415082-T-G

32450387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21415373-G-A

32450444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21415427-G-A

http://identifiers.org/hco/18/GRCh38#32452327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21416585-A-C

32452364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21416625-G-A

http://identifiers.org/hco/18/GRCh38#32452365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21416626-C-A

32452365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21416626-C-T

32452643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21416923-G-A

32452714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21416993-C-T

32452926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21417182-G-A

32453433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21417287-G-A

32453660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21417504-G-T

32453765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21417608-C-T

32453861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21417723-T-C

32455104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21419133-T-C

32455158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21419184-A-G

32455221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21419236-G-A

32455221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21419236-G-T

32455437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21419450-C-T

32455566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21419610-T-C

32455570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21419614-T-C

32456150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21420211-C-G

32456274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21420327-C-T

32456528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21420637-C-T

32456592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21420699-C-T

32457390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21421456-C-T

32457397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21421463-T-C

32457741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21421764-G-A

32458037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21421946-T-G

32458338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21422042-G-A

32458612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21422213-A-G

32459196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21422776-G-A

32459453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21423772-C-G

32459453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21423772-C-T

32459582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21423898-G-C

32460192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21424486-A-G

32460263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21424554-A-G

32460683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21424940-C-G

32460912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21425170-C-T

32461187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21425299-T-G

32461325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21425440-A-G

32461783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21425602-C-T

32464575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21426323-T-C

32464616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21426361-G-A

32464852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21426658-A-G

32464992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21426755-G-A

32465056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21426818-T-G

32465123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21426859-A-G

32465135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21426871-C-T

32465156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21426896-C-G

32465172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21426915-T-C

32466177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21428270-T-A

32466279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21428368-G-A

32466279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21428368-G-C

http://identifiers.org/hco/18/GRCh38#32466959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21429269-A-C

32467212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21429715-C-T

32467214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21429717-C-G

http://identifiers.org/hco/18/GRCh38#32467382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21429884-C-A

32467774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21430237-G-A

32467923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21430389-T-A

32468009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21430470-G-C

32468164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21430623-C-T

32468267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21430749-A-G

32468315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21430801-C-T

32468884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21431350-G-A

http://identifiers.org/hco/18/GRCh38#32468967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21431411-C-A

32468967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21431411-C-G

32468967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21431411-C-T

32469063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21431494-A-G

32469247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21431672-C-T

32469924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21432375-C-T

32470146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21432564-A-G

32470146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron variant
orthologous variants: 21432564-A-T

32470191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21432608-C-G

32470191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21432608-C-T

http://identifiers.org/hco/18/GRCh38#32470225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#21432646-C-A

32470225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21432646-C-T

http://identifiers.org/hco/18/GRCh38#32470226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#21432647-C-A

32470226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21432647-C-G

32470226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21432647-C-T

32470231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21432652-T-C

http://identifiers.org/hco/18/GRCh38#32470240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#21432661-C-A

32470240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21432661-C-T

http://identifiers.org/hco/18/GRCh38#32470242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#21432663-C-A

32470242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21432663-C-G

32470242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21432663-C-T

32470243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21432664-G-A

32470243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, undefined
orthologous variants: 21432664-G-T

http://identifiers.org/hco/18/GRCh38#32470387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#21432786-C-A

32470387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21432786-C-T

32470405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21432804-G-A

32470405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21432804-G-C

32470405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21432804-G-T

32470473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21432872-G-A

32470473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21432872-G-C

32470583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21432937-G-A

http://identifiers.org/hco/18/GRCh38#32470602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#21432940-C-A

32470602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21432940-C-G

32470602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21432940-C-T

32470644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21432981-G-C

32470849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26136
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21433163-G-C