http://identifiers.org/hco/22/GRCh38#43955451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#84076474-C-A

43955451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84076474-C-T

43955552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84076539-G-A

43955552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84076539-G-T

http://identifiers.org/hco/22/GRCh38#43955553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#84076540-C-A

43955553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84076540-C-T

43960039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84077865-G-T

43960115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84077939-A-G

43960265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84078094-A-T

43960284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84078116-C-T

http://identifiers.org/hco/22/GRCh38#43962931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#84079601-C-A

43962931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84079601-C-T

43962932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84079602-G-A

43962932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84079602-G-T

http://identifiers.org/hco/22/GRCh38#43962991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#84079664-C-A

43962993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84079665-G-A

43963020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84079692-C-T

http://identifiers.org/hco/22/GRCh38#43963040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#84079701-C-A

43963042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84079703-T-C

http://identifiers.org/hco/22/GRCh38#43963078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#84079748-A-C

43963078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84079748-A-G

43963086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84079764-A-T

43963127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84079805-G-A

43963127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84079805-G-T

http://identifiers.org/hco/22/GRCh38#43963147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#84079820-C-A

43963147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84079820-C-G

43963147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84079820-C-T

43963169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84079846-A-G

http://identifiers.org/hco/22/GRCh38#43963174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#84079851-A-C

43963174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84079851-A-G

43963268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84079927-T-A

43963280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 84079939-T-C

43963369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 84080028-T-C

43963463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84080116-G-A

http://identifiers.org/hco/22/GRCh38#43963525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#84080148-C-A

43963525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84080148-C-T

43964308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84081057-T-C

43964348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84081107-G-A

43964348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84081107-G-T

43964466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 84081220-T-C

43964587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84081341-G-A

43964587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84081341-G-C

43964587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84081341-G-T

43964646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84081381-G-A

43964646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84081381-G-T

43964748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84081425-C-T

http://identifiers.org/hco/22/GRCh38#43964938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84081552-C-A

43964938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84081552-C-T

43964940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84081554-C-G

43964946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84081560-C-G

http://identifiers.org/hco/22/GRCh38#43965145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84081732-C-A

43968685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84082732-T-C

43968685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84082732-T-G

43968748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 84082792-T-C

43968811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 84082855-A-G

43972219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84083957-A-T

43972230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 84083968-A-G

43972230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 84083968-A-T

43972349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 84084087-T-C

43972350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 84084088-A-G

43972354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84084091-G-A

43972354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84084091-G-C

43972354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84084091-G-T

43972401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84084134-T-A

43972401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84084134-T-C

43972845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84084466-G-T

http://identifiers.org/hco/22/GRCh38#43972863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84084484-C-A

43972863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 84084484-C-T

43972906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 84084529-T-G

43972966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 84084589-C-G

43973036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84084659-C-G

43973036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84084659-C-T

43973047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84084670-G-A

43973065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84084688-T-C

http://identifiers.org/hco/22/GRCh38#43973096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84084714-C-A

43973096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84084714-C-T

http://identifiers.org/hco/22/GRCh38#43973105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84084723-C-A

43973113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84084731-A-G

43973150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84084752-G-A

43973153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84084755-G-A

43973153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84084755-G-T

http://identifiers.org/hco/22/GRCh38#43973190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84084791-C-A

43973190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84084791-C-G

43973190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84084791-C-T

43973199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84084795-G-T

http://identifiers.org/hco/22/GRCh38#43973222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84084817-C-A

43973222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84084817-C-T

43973385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron variant
orthologous variants: 84084979-A-G

43973385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron variant
orthologous variants: 84084979-A-T

http://identifiers.org/hco/22/GRCh38#43973475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84085026-C-A

43973475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron variant
orthologous variants: 84085026-C-T

43973542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron variant
orthologous variants: 84085097-G-A

http://identifiers.org/hco/22/GRCh38#43974873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84085194-A-C

43974873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84085194-A-G

43974927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84085246-T-C

43975100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84085500-A-G

43975114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84085514-A-G

43975123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84085523-A-G

http://identifiers.org/hco/22/GRCh38#43975174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84085560-C-A

43975174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84085560-C-T

43975211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84085599-G-A

43975211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84085599-G-T

43975226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84085613-T-C

43975226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84085613-T-G

43975254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84085657-G-A

43975254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84085657-G-T

43975322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84085718-A-G

http://identifiers.org/hco/22/GRCh38#43975424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84085805-C-A

http://identifiers.org/hco/22/GRCh38#43975425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84085806-A-C

43975430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84085811-T-C

43975520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84085884-G-T

43975572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84085929-G-A

http://identifiers.org/hco/22/GRCh38#43975581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84085938-C-A

43975581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84085938-C-T

43975592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84085949-C-T

43975602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84085959-G-A

43975602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84085959-G-T

http://identifiers.org/hco/22/GRCh38#43975606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84085963-C-A

43975606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84085963-C-T

43975629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84085982-T-G

43975665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086022-G-A

43975665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086022-G-T

43975667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086024-G-A

43975667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086024-G-T

43975684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086038-G-T

43975691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086042-C-T

43975692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086043-G-A

43975692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086043-G-T

http://identifiers.org/hco/22/GRCh38#43975694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84086045-C-A

43975694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086045-C-T

http://identifiers.org/hco/22/GRCh38#43975749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84086085-C-A

43975749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086085-C-G

43975749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086085-C-T

43975752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086088-G-A

43975752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086088-G-T

http://identifiers.org/hco/22/GRCh38#43975789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84086121-C-A

43975789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086121-C-T

http://identifiers.org/hco/22/GRCh38#43975795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84086127-C-A

43975795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086127-C-T

43975849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086168-A-G

43975849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086168-A-T

http://identifiers.org/hco/22/GRCh38#43975853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84086172-C-A

43975854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086173-T-A

43975854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086173-T-C

http://identifiers.org/hco/22/GRCh38#43975884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84086200-C-A

http://identifiers.org/hco/22/GRCh38#43975894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84086210-C-A

43975894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086210-C-T

43975912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086233-T-C

http://identifiers.org/hco/22/GRCh38#43975924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84086279-C-A

43975924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086279-C-T

43975964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086337-A-G

43975964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086337-A-T

43976013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086387-A-G

43976031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84086405-A-G

http://identifiers.org/hco/22/GRCh38#43976063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84086439-A-C

43976063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 84086439-A-G

43976251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84086616-G-A

http://identifiers.org/hco/22/GRCh38#43976270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84086634-C-A

43976272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84086636-G-A

43976451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84086731-C-T

http://identifiers.org/hco/22/GRCh38#43976473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84086751-C-A

43976490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84086768-C-G

43976497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84086776-G-A

43976583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84086835-A-G

http://identifiers.org/hco/22/GRCh38#43976624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84086868-C-A

43976624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84086868-C-G

43976624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84086868-C-T

43976669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84086901-G-A

43976683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84086915-G-A

43976866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84087080-A-G

43976893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84087158-T-G

43980774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84090526-G-A

43980903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84090668-G-A

43980944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84090690-T-C

43980948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84090694-G-C

43981088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84090815-C-T

http://identifiers.org/hco/22/GRCh38#43981278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84090966-C-A

43981278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84090966-C-T

43981381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84091062-A-G

43981465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84091146-A-T

43981585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84091230-G-A

43981585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84091230-G-T

43981637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84091279-T-C

43989095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84094674-C-T

43989160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 84094734-C-T

43990454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84095410-A-G

43990455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84095411-T-C

43990468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84095424-T-C

43990468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84095424-T-G

http://identifiers.org/hco/22/GRCh38#43990472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84095428-C-A

43990472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84095428-C-T

43990549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84095505-T-C

43990627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84095568-G-A

http://identifiers.org/hco/22/GRCh38#43993304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#84096529-C-A

43993304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84096529-C-T

43993736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84096927-G-A

43993747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84096939-A-G

43993881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84097055-A-G

43994015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84097181-G-A

43996275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84098276-G-A

43996305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84098298-G-A

http://identifiers.org/hco/22/GRCh38#43996422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84098401-C-A

43996422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84098401-C-T

43996464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84098444-G-A

43996464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84098444-G-C

43996464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84098444-G-T

43996483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84098462-T-C

43996483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84098462-T-G

http://identifiers.org/hco/22/GRCh38#43996525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84098500-C-A

43996525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84098500-C-T

43998362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84100748-T-C

43998852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84101140-G-A

43998863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84101151-G-A

44002568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84102427-G-C

44002568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84102427-G-T

http://identifiers.org/hco/22/GRCh38#44002702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#84102520-A-C

44002702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84102520-A-G

44002738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84102551-G-A

44002831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84102628-G-A

44002917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84102712-C-G

44002917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84102712-C-T

44002957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84102752-G-A

44002996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84102794-C-T

44003112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84102899-C-T

44003169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84102954-G-A

44003384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84103175-T-C

44003389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84103180-G-A

44003453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84103231-A-G

44003508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84103282-T-C

44003696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84103444-C-T

44003814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84103571-T-G

44009202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84106197-C-T

44009501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84106901-C-T