11199412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21711570-G-C

11199418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21711576-A-G

http://identifiers.org/hco/19/GRCh38#11199447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21711609-C-A

11199447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21711609-C-T

http://identifiers.org/hco/19/GRCh38#11199480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21711641-C-A

11199480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21711641-C-T

11199521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21711677-T-C

11199592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21711742-A-G

11199592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21711742-A-T

http://identifiers.org/hco/19/GRCh38#11199625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21711770-C-A

11199625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21711770-C-T

11199627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21711772-T-C

http://identifiers.org/hco/19/GRCh38#11199638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21711783-C-A

11199638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21711783-C-T

11199682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21711858-G-A

11199682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21711858-G-T

11199710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21711886-C-T

11199712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21711888-C-T

11200207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21712429-T-A

11200207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21712429-T-C

http://identifiers.org/hco/19/GRCh38#11200383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21712542-C-A

11200383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21712542-C-T

http://identifiers.org/hco/19/GRCh38#11200395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21712554-C-A

11200395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21712554-C-T

http://identifiers.org/hco/19/GRCh38#11200433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21712592-A-C

11200433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21712592-A-G

11200433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21712592-A-T

11200478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21712638-C-T

11200487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21712647-G-A

11200491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21712651-A-G

11200491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21712651-A-T

11200502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21712658-C-G

11200502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21712658-C-T

11200647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21712768-G-C

11200648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21712769-A-G

http://identifiers.org/hco/19/GRCh38#11200696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21712812-C-A

11200696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21712812-C-G

11200832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21712934-G-A

11200880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21712979-G-A

http://identifiers.org/hco/19/GRCh38#11200898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21713010-A-C

11200898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21713010-A-G

11200899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21713011-C-T

11201073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21713184-T-C

11201143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21713290-T-A

11201143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21713290-T-C

http://identifiers.org/hco/19/GRCh38#11201172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21713312-A-C

11201172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21713312-A-T

11201180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21713327-T-G

11201205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21713353-G-C

11201254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21713401-G-T

11201262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21713409-C-T

11201271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21713418-C-G

11201289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21713436-C-T

11201335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21713469-C-T

http://identifiers.org/hco/19/GRCh38#11201805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21713608-C-A

11201805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21713608-C-T

http://identifiers.org/hco/19/GRCh38#11201807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21713610-C-A

11201809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21713612-G-A

11201809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21713612-G-T

http://identifiers.org/hco/19/GRCh38#11201813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21713616-C-A

11201898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21713658-G-T

11201976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21713736-G-A

11201976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21713736-G-C

11202006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21713766-C-T

11202021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21713781-G-T

11202051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21713811-G-C

11202060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21713820-G-C

11202096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21713856-C-G

11202096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21713856-C-T

11202154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21713940-C-T

11202180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21713958-C-G

11202202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21713981-T-A

11202202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21713981-T-C

11202233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21714010-A-G

http://identifiers.org/hco/19/GRCh38#11202571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21714276-C-A

11202695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21714400-C-G

11202695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21714400-C-T

11202733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21714438-G-A

11202816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21714527-A-T

11203080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21714961-G-A

11203151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21715096-T-C

http://identifiers.org/hco/19/GRCh38#11203166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21715111-C-A

11203166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21715111-C-T

http://identifiers.org/hco/19/GRCh38#11203225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21715170-C-A

11203257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21715193-G-A

11203257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21715193-G-T

11203289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21715225-G-A

11203289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21715225-G-T

11203306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21715242-G-A

11203306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21715242-G-T

http://identifiers.org/hco/19/GRCh38#11203446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21715394-C-A

11203446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21715394-C-G

11203446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21715394-C-T

11203520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21715450-G-A

11203520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21715450-G-T

11203657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21715571-G-T

11203939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21715806-G-T

11203940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21715807-G-A

11203954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21715820-G-A

11203954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21715820-G-T

11203972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21715840-A-G

11204149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21715968-G-C

11204175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21715990-T-C

11204175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21715990-T-G

11204186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21716001-G-A

11204186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21716001-G-T

11204187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21716002-G-A

11204187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21716002-G-T

11204248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21716063-G-A

11204248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21716063-G-T

http://identifiers.org/hco/19/GRCh38#11204436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21716221-C-A

11204436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21716221-C-T

11207110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21718687-G-A

11207110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21718687-G-C

11207450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21719007-C-T

11207476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21719033-A-G

http://identifiers.org/hco/19/GRCh38#11208391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21720567-C-A

http://identifiers.org/hco/19/GRCh38#11208400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21720576-C-A

11208402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21720578-T-C

http://identifiers.org/hco/19/GRCh38#11208410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21720580-A-C

11208416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21720586-G-A

11208416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21720586-G-C

11208418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21720588-T-C

11208418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21720588-T-G

http://identifiers.org/hco/19/GRCh38#11208425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21720595-C-A

11208425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21720595-C-T

11208476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21720643-T-A

11208496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21720661-G-A

11208496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21720661-G-T

11208559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21720697-G-A

11208559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21720697-G-T

http://identifiers.org/hco/19/GRCh38#11208578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21720715-C-A

http://identifiers.org/hco/19/GRCh38#11208586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21720723-C-A

11208586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21720723-C-T

http://identifiers.org/hco/19/GRCh38#11208605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21720742-C-A

11208605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21720742-C-T

http://identifiers.org/hco/19/GRCh38#11208677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21720808-A-C

11208677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21720808-A-G

11208677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21720808-A-T

11208699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21720830-C-T

http://identifiers.org/hco/19/GRCh38#11209015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21721148-C-A

11209015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 21721148-C-T

11209117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21721250-G-T

11209154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21721289-C-T

11209176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21721308-T-C

http://identifiers.org/hco/19/GRCh38#11209191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21721330-A-C

11209191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21721330-A-G

http://identifiers.org/hco/19/GRCh38#11209214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21721355-C-A

11209214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21721355-C-T

11209215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21721356-A-G

http://identifiers.org/hco/19/GRCh38#11209236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21721377-C-A

11209236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21721377-C-G

11209236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21721377-C-T

11211662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21722994-A-G

11211704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21723030-A-G

11211704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21723030-A-T

http://identifiers.org/hco/19/GRCh38#11211709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21723035-C-A

11211709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21723035-C-T

11211717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21723043-T-C

http://identifiers.org/hco/19/GRCh38#11211758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21723059-C-A

11211758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21723059-C-T

11211802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21723096-A-G

11211855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21723149-G-A

11211855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 21723149-G-C

11211855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 21723149-G-T

11211899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21723193-G-A

11211936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21723204-T-G

11211940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21723208-G-A

11211940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21723208-G-T

11211953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21723220-A-G

11211953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21723220-A-T

11211957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21723224-G-A

11211957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21723224-G-C

11211957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21723224-G-T

11212025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 21724280-T-C

11212156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21724411-A-G

11212156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21724411-A-T

11212169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21724423-G-A

http://identifiers.org/hco/19/GRCh38#11212195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21724449-C-A

http://identifiers.org/hco/19/GRCh38#11212220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21724476-C-A

11212234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21724489-G-A

11212234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21724489-G-T

http://identifiers.org/hco/19/GRCh38#11212237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21724492-C-A

11212237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21724492-C-T

11213221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21724726-G-A

11213221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 21724726-G-T

11213414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21724904-G-A

11213414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21724904-G-T

11213773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21725302-G-A

11213774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21725303-T-C

11213797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21725326-T-A

11213903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21725419-C-T

11213909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21725423-C-G

11213943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21725485-C-T

11214021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21725575-G-C

11214040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21725597-C-T

11214098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21725667-T-G

11214215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21725724-G-A

11214215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21725724-G-C

11214215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21725724-G-T

11214254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21725741-T-G

11214368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21725858-T-C

11214421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21725905-G-A

11214484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21725943-T-G

11214485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21725944-G-A

http://identifiers.org/hco/19/GRCh38#11214499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21725958-C-A

11214499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21725958-C-G

11214558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 21726012-C-T

11214563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 21726017-A-G

11214563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 21726017-A-T

11214663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21726116-G-A

11214671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21726124-T-C

11214686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21726137-G-A

http://identifiers.org/hco/19/GRCh38#11214724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21726178-C-A

11214724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21726178-C-G

11214724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21726178-C-T

http://identifiers.org/hco/19/GRCh38#11215431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21727241-C-A

11215578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21727385-G-C

11215578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21727385-G-T

11215632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21727435-T-C

11215664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21727455-G-A

11215664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21727455-G-C

11215664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21727455-G-T

11215671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21727462-A-G

11215687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21727475-C-G

11215698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21727486-G-A

11215701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21727489-G-A

11215701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21727489-G-T

11215976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21727760-G-A

11215976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21727760-G-T

http://identifiers.org/hco/19/GRCh38#11216383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21728157-A-C

11216521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21728265-T-C

http://identifiers.org/hco/19/GRCh38#11216534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21728271-A-C

11216534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21728271-A-G

http://identifiers.org/hco/19/GRCh38#11216549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21728286-A-C

11216549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21728286-A-G

11216566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21728303-C-G

11216566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21728303-C-T

11216570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21728307-G-T

11216644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21728372-G-A

11216644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21728372-G-T

11216661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21728389-G-A

11216661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21728389-G-T

11216662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21728390-G-A

11216662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21728390-G-C

11216662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21728390-G-T

11216821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21728490-G-T

11216907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21728572-C-G

11217010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21728675-C-G

11217010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21728675-C-T

11217100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21728765-G-A

11217100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21728765-G-T

11217118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21728783-A-G

http://identifiers.org/hco/19/GRCh38#11217156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21728821-C-A

11217156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21728821-C-T

11217191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21728975-A-G

11217207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21729086-A-G

11217312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: synonymous variant
orthologous variants: 21729190-G-A

11217411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21729282-G-A

11222044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21731752-G-A

11222046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21731754-C-T

11222103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21731812-G-A

11222257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21731973-T-G

http://identifiers.org/hco/19/GRCh38#11222277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21732043-C-A

11222277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21732043-C-T

11222334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21732149-G-C

11222369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21732253-G-T

11222371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21732255-T-C

11222394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21732313-G-T

11222601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21732632-G-T

11222747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 21732764-G-A

11222747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 21732764-G-T

http://identifiers.org/hco/19/GRCh38#11222756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21732773-A-C

11222756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 21732773-A-G

11222822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 21732839-G-A

11222822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 21732839-G-T

11222855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 21732872-C-T

11222981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21733003-G-A

11223038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: 3_prime_UTR_variant, stop_gained, synonymous_variant
orthologous variants: 21733076-C-T

11223162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21733211-C-T

http://identifiers.org/hco/19/GRCh38#11223167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21733216-C-A

11223167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21733216-C-G

11223167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21733216-C-T

http://identifiers.org/hco/19/GRCh38#11223183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21733265-C-A

11223198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21733290-G-A

11223198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21733290-G-T

11223227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21733315-G-A

11223227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21733315-G-T

11223474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21733614-G-A

11225544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21734285-T-G

11225910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21734745-G-C

11226042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21734859-C-T

http://identifiers.org/hco/19/GRCh38#11226089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21734919-C-A

11226782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21735240-G-T

11226794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21735252-G-C

11226922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21735374-A-G

11226942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21735394-T-C

11227348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: missense variant
orthologous variants: 21735704-G-A

11227388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 21735744-G-A

11227506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21735874-G-A

11227506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21735874-G-T

11227558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21735923-G-A

11227563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21735928-G-A

11227563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21735928-G-T

http://identifiers.org/hco/19/GRCh38#11228893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21736671-C-A

11228985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21736776-T-G

11229069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21736859-G-A

11229069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21736859-G-T

http://identifiers.org/hco/19/GRCh38#11229104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21736895-C-A

11229104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21736895-C-T

11229106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21736903-A-G

11229230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21737006-G-A

11229230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21737006-G-T

11229263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21737042-A-G

11229318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21737099-G-T

11229352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21737133-G-A

11229456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21737254-G-A

11229456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21737254-G-T

http://identifiers.org/hco/19/GRCh38#11229471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21737269-C-A

11229485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21737284-G-A

11229485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21737284-G-T

11229545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21737344-G-C

11231992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21740595-T-C

11232106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21740696-G-A

11232106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21740696-G-C

11232106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21740696-G-T

11232148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21740735-G-T

11232216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant
orthologous variants: 21740801-G-A

11232284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21740869-G-A

11232284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21740869-G-T

11232314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21740899-G-C

http://identifiers.org/hco/19/GRCh38#11232316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21740901-A-C

11232530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21741074-T-A

http://identifiers.org/hco/19/GRCh38#11233083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21741419-A-C

http://identifiers.org/hco/19/GRCh38#11233415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21741690-C-A

11233415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21741690-C-G

11233415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21741690-C-T

11233468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21741741-G-A

11233486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21741757-T-C

11233506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21741780-G-A

11233506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21741780-G-T

11235644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: synonymous variant
orthologous variants: 21742375-G-T

11236239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21742561-G-C

11236239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21742561-G-T

11236264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21742586-G-A

11236264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21742586-G-T

http://identifiers.org/hco/19/GRCh38#11236302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21742622-C-A

11236302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21742622-C-T

http://identifiers.org/hco/19/GRCh38#11236371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21742733-C-A

11236371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21742733-C-G

11236371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21742733-C-T

11236491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21742853-G-A

11236491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21742853-G-T

http://identifiers.org/hco/19/GRCh38#11236512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21742874-C-A

11236512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21742874-C-T

11236590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21742952-G-A

11236639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 21743001-A-G

http://identifiers.org/hco/19/GRCh38#11236687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#21743037-C-A

11236696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 21743047-A-G

11236814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21743171-G-A

11236814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21743171-G-C

11236814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21743171-G-T

http://identifiers.org/hco/19/GRCh38#11236874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#21743231-C-A

11236874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 21743231-C-T

11236940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21743334-A-G

11236941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21743335-G-T

http://identifiers.org/hco/19/GRCh38#11236981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21743376-C-A

11236981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21743376-C-T

http://identifiers.org/hco/19/GRCh38#11237003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#21743402-A-C

http://identifiers.org/hco/19/GRCh38#11237032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21743431-C-A

http://identifiers.org/hco/19/GRCh38#11237060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#21743461-A-C

http://identifiers.org/hco/19/GRCh38#11237064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#21743465-A-C

11237064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 21743465-A-G

http://identifiers.org/hco/19/GRCh38#11237075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#21743473-C-A

11237075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 21743473-C-T

11237076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 21743474-G-A

11237076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 21743474-G-T

11237103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21743519-A-G

11237119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 21743541-G-T

11237143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21743576-G-A

http://identifiers.org/hco/19/GRCh38#11237213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21743794-C-A

11237213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21743794-C-G

11237213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21743794-C-T

11237280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21743947-G-A

11237280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21743947-G-T

http://identifiers.org/hco/19/GRCh38#11237296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21743963-C-A

http://identifiers.org/hco/19/GRCh38#11237332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#21743995-C-A

11237332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 21743995-C-G

11237332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 21743995-C-T

11237419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744097-A-G

11237656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21744346-T-C

11237734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21744424-G-A

11237734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 21744424-G-T

11237805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744490-G-A

11237805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744490-G-T

11237814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744508-T-A

11237814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744508-T-C

11237815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744509-G-A

11237815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744509-G-T

11237826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744520-T-C

11237827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744521-G-A

11237827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744521-G-C

11237827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744521-G-T

http://identifiers.org/hco/19/GRCh38#11237829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21744523-C-A

11237829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744523-C-T

11237893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744533-G-T

http://identifiers.org/hco/19/GRCh38#11237966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21744581-C-A

11237966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744581-C-T

11237993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744598-T-G

11237994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744599-C-T

11238017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744618-C-G

11238017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744618-C-T

11238187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 21744820-C-T

11238211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21744844-G-A

11238314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744947-G-A

11238314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744947-G-C

11238314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744947-G-T

11238338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744962-A-G

11238338-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21744962-A-T

11238480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21745061-G-T

11238486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21745067-G-A

11238486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21745067-G-C

11238486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21745067-G-T

11239199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21746386-T-C

11239295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21746471-C-T

11239513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, undefined
orthologous variants: 21746696-T-C

11239687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant
orthologous variants: 21746863-G-A

11239691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 21746867-T-C

11239694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 21746870-C-T

11239697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 21746873-A-G

11239991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21747136-G-A

11239991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21747136-G-T

11240212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 21747289-G-A

11240212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 21747289-G-T

11240223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant
orthologous variants: 21747300-G-A

11240223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant
orthologous variants: 21747300-G-C

11240223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant
orthologous variants: 21747300-G-T

11240357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21747432-T-G

11241335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21748030-G-T

11241364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21748059-A-G

11241366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21748061-A-G

11241366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21748061-A-T

11241410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21748106-G-A

11241410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21748106-G-T

11241422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21748118-G-T

http://identifiers.org/hco/19/GRCh38#11241538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21748232-C-A

11241538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, stop_gained
orthologous variants: 21748232-C-T

11241582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21748275-G-T

11241638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21748334-T-C

11241669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21748365-A-G

11241669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21748365-A-T

11241705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21748401-T-C

11241823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21748520-A-G

11241839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21748540-G-A

11241839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21748540-G-T

http://identifiers.org/hco/19/GRCh38#11241897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21748597-C-A

11241897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21748597-C-T

http://identifiers.org/hco/19/GRCh38#11241926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21748626-C-A

11242037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 21750039-G-C

11242176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: synonymous variant
orthologous variants: 21750178-A-G

11242215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 21750217-G-A

11242215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 21750217-G-T

http://identifiers.org/hco/19/GRCh38#11242231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21750233-C-A

11242231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21750233-C-T

11242270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21750250-G-A

11242270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21750250-G-T

11243017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21750395-G-C

11243017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21750395-G-T

11243060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 21750440-A-G

11243143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: stop gained
orthologous variants: 21750523-G-A

11243143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: missense variant
orthologous variants: 21750523-G-C

11243221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21750597-G-A

11243408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, undefined
orthologous variants: 21750799-C-T

http://identifiers.org/hco/19/GRCh38#11243546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#21750910-C-A

11243546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, undefined
orthologous variants: 21750910-C-T

http://identifiers.org/hco/19/GRCh38#11243548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#21750912-C-A

11243548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, undefined
orthologous variants: 21750912-C-T

11243570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: synonymous_variant, undefined
orthologous variants: 21750934-A-G

11243614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: synonymous_variant, undefined
orthologous variants: 21750972-A-G

11243614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: missense_variant, undefined
orthologous variants: 21750972-A-T

http://identifiers.org/hco/19/GRCh38#11243624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#21750982-C-A

11243624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: synonymous_variant, undefined
orthologous variants: 21750982-C-T

11243795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 21751161-C-G

11243795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 21751161-C-T

11243806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: missense variant
orthologous variants: 21751172-G-A

11243914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21751276-G-A

11243914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21751276-G-T

11243925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21751287-G-A

11243925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21751287-G-C

11243970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21751313-G-T

11243971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21751314-G-A

11243978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21751321-G-A

11243978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21751321-G-T

11244022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21751403-G-A

11244025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21751406-T-C

11244025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21751406-T-G

11245073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21752485-C-G

http://identifiers.org/hco/19/GRCh38#11245560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21752786-C-A

11245560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21752786-C-T

11245778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21753114-G-A

11245897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21753291-G-A

11245897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21753291-G-T

http://identifiers.org/hco/19/GRCh38#11245928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21753311-C-A

11245928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21753311-C-T

http://identifiers.org/hco/19/GRCh38#11245935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21753318-C-A

11245935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron variant
orthologous variants: 21753318-C-T

http://identifiers.org/hco/19/GRCh38#11248155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21754326-C-A

11248155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21754326-C-T

http://identifiers.org/hco/19/GRCh38#11248157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21754328-A-C

11248157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21754328-A-G

http://identifiers.org/hco/19/GRCh38#11248240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21754465-A-C

11248240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21754465-A-G

11248253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21754478-T-A

11248253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21754478-T-C

11249020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21755218-A-G

11249020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21755218-A-T

11249115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21755295-G-A

11251033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21755662-A-G

11251096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21755724-G-A

11251096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21755724-G-T

11251148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21755769-T-A

11251148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21755769-T-C

http://identifiers.org/hco/19/GRCh38#11251212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21755839-C-A

11251212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21755839-C-T

11251290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21755919-G-T

11251293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21755922-G-A

11251389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21756053-G-A

http://identifiers.org/hco/19/GRCh38#11251401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21756065-C-A

11251401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21756065-C-T

11251434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21756096-G-A

11251434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21756096-G-T

11251441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21756103-G-A

11251441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21756103-G-T

http://identifiers.org/hco/19/GRCh38#11251472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21756153-C-A

http://identifiers.org/hco/19/GRCh38#11251490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21756188-C-A

11251493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21756191-A-G

http://identifiers.org/hco/19/GRCh38#11251734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21756388-A-C

11251734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21756388-A-G

11251796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21756425-G-A

11251796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21756425-G-T

http://identifiers.org/hco/19/GRCh38#11251850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21756471-C-A

11251850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21756471-C-T

http://identifiers.org/hco/19/GRCh38#11251855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21756476-C-A

11251855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21756476-C-T

http://identifiers.org/hco/19/GRCh38#11252061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21756675-C-A

11252061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21756675-C-T

11252093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21756715-G-A

11252095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21756717-G-A

11252095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21756717-G-T

11252106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21756728-G-A

11252106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21756728-G-C

11252106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21756728-G-T

11252107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21756729-G-A

11252107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21756729-G-C

11252107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21756729-G-T

11252109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21756731-G-A

11252109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21756731-G-T

http://identifiers.org/hco/19/GRCh38#11252113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21756734-C-A

11252113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21756734-C-T

http://identifiers.org/hco/19/GRCh38#11252138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21756759-C-A

11252138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21756759-C-T

11252155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21756776-A-T

11252193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 21756814-G-A

11252193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21756814-G-C

11252193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21756814-G-T

http://identifiers.org/hco/19/GRCh38#11252197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21756818-C-A

11252197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21756818-C-T

11252278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21756903-G-T

http://identifiers.org/hco/19/GRCh38#11252374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21756961-C-A

11252374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21756961-C-T

11252478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21757053-T-A

11252523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21757098-C-T

http://identifiers.org/hco/19/GRCh38#11252822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21757834-C-A

11252822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21757834-C-G

11252822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21757834-C-T

11252947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21757959-A-G

11252947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21757959-A-T

11253000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21758010-G-A

11253000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21758010-G-T

11253064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21758055-G-A

11253064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21758055-G-T

http://identifiers.org/hco/19/GRCh38#11253072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21758065-C-A

http://identifiers.org/hco/19/GRCh38#11253329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21758276-C-A

11253333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21758280-A-G

11253398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21758316-G-A

11253490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21758411-T-A

11253490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21758411-T-C

11253490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21758411-T-G

11253547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21758429-G-A

11253547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21758429-G-T

11253557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21758439-G-A

11253557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21758439-G-T

http://identifiers.org/hco/19/GRCh38#11253681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21758523-A-C

11253681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21758523-A-G

11253681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21758523-A-T

11253769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21758610-G-A

11253769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21758610-G-C

11253769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21758610-G-T

11253797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21758648-G-A

11253797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21758648-G-T

11253809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21758660-G-A

11253809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21758660-G-T

11253870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21758724-G-A

http://identifiers.org/hco/19/GRCh38#11253881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21758746-C-A

11253881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21758746-C-T

http://identifiers.org/hco/19/GRCh38#11253895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21758758-A-C

11253895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21758758-A-G

11253923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21758790-A-G

11253923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21758790-A-T

11261383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21763227-G-A

11261383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21763227-G-C

11261794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21763545-G-A

11262258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21763805-G-A

11262258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21763805-G-C

11262258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21763805-G-T

http://identifiers.org/hco/19/GRCh38#11262288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21763825-A-C

11262288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21763825-A-G

11262288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21763825-A-T

11262487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19189
most severe consequence: 5 prime UTR variant
orthologous variants: 21763899-C-T